This rubric evaluates software based on 9 criteria: content, design, functionality, instructional design, interactivity, assessment, usability, technology, and accessibility. Software receives higher scores for providing accurate, reliable content aligned to standards. It also scores well for intuitive navigation, multimedia enhancements, feedback and support for learners, and easy integration into classroom activities. The rubric assesses whether the software engages students and allows teachers to track progress.
This presentation is aimed at providing information on automation in the GLP practices in the pharmaceutical industry.
-Standard Operating Procedures.
-Documentation in GALP.
-Logs and Related Forms.
21 CFR-FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES...ICHAPPS
TRAINING PROGRAMME ON
21CFR PARTS-210 AND 211
QUALITY ASSURANCE
Slideshow About 21 CFR
“Every product must be fit for its intended purpose”
“Every product must be fit for its intended purpose”
FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES- UNITED STATES OF AMERICA
The document discusses guidelines for supplemental new drug applications (sNDAs) according to the US FDA. It outlines three categories of variations - major, moderate, and minor - based on their potential impact. Major changes require prior approval and could impact safety or efficacy. Moderate changes require submission 30 days before distribution or upon FDA receipt. Minor changes only require description in the annual report. The document provides examples of changes in manufacturing sites, processes, specifications, container closure systems, and labeling that would fall under each category. Close monitoring and reporting of any post-approval changes is recommended to ensure the quality, safety and efficacy of pre-qualified products are not adversely affected.
This document summarizes the objectives and classification system of the Global Harmonization Task Force (GHTF) for in vitro diagnostic (IVD) medical devices. The GHTF was founded in 1993 to harmonize medical device regulations globally. It aims to facilitate trade while preserving public health. IVD medical devices are classified into 4 risk-based classes (A to D) based on 16 general rules related to device invasiveness, energy use, and disease detection. Class A devices pose the lowest risk while Class D the highest. The classification system aims to ensure regulatory oversight is proportionate to device risk.
A brief presentation on the current good manufacturing practices employed in the manufacture of pharmaceuticals in the US.
Comprises of all aspects of good manufacturing practices
This document provides a checklist for compliance with 21 CFR Part 11, which establishes criteria for electronic records and electronic signatures. It discusses the need for validation, audit trails, electronic signatures, copies of records, and record retention. Each section provides points to evaluate like ensuring limited system access, time-stamped audit trails, unique electronic signatures, and the ability to produce accurate copies of electronic records. The document aims to help organizations evaluate their systems and processes to ensure compliance with FDA regulations for electronic records.
This document discusses various post-approval requirements and processes for pharmaceutical drugs, including prior approval supplements, changes being effected in 30 days supplements, annual reports, labeling changes, recalls, FDA inspections, and ISO 31000 risk management standards. It provides details on submission requirements and timelines for different types of post-approval changes, as well as FDA enforcement actions like warning letters, seizures, and injunctions.
This presentation is aimed at providing information on automation in the GLP practices in the pharmaceutical industry.
-Standard Operating Procedures.
-Documentation in GALP.
-Logs and Related Forms.
21 CFR-FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES...ICHAPPS
TRAINING PROGRAMME ON
21CFR PARTS-210 AND 211
QUALITY ASSURANCE
Slideshow About 21 CFR
“Every product must be fit for its intended purpose”
“Every product must be fit for its intended purpose”
FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES- UNITED STATES OF AMERICA
The document discusses guidelines for supplemental new drug applications (sNDAs) according to the US FDA. It outlines three categories of variations - major, moderate, and minor - based on their potential impact. Major changes require prior approval and could impact safety or efficacy. Moderate changes require submission 30 days before distribution or upon FDA receipt. Minor changes only require description in the annual report. The document provides examples of changes in manufacturing sites, processes, specifications, container closure systems, and labeling that would fall under each category. Close monitoring and reporting of any post-approval changes is recommended to ensure the quality, safety and efficacy of pre-qualified products are not adversely affected.
This document summarizes the objectives and classification system of the Global Harmonization Task Force (GHTF) for in vitro diagnostic (IVD) medical devices. The GHTF was founded in 1993 to harmonize medical device regulations globally. It aims to facilitate trade while preserving public health. IVD medical devices are classified into 4 risk-based classes (A to D) based on 16 general rules related to device invasiveness, energy use, and disease detection. Class A devices pose the lowest risk while Class D the highest. The classification system aims to ensure regulatory oversight is proportionate to device risk.
A brief presentation on the current good manufacturing practices employed in the manufacture of pharmaceuticals in the US.
Comprises of all aspects of good manufacturing practices
This document provides a checklist for compliance with 21 CFR Part 11, which establishes criteria for electronic records and electronic signatures. It discusses the need for validation, audit trails, electronic signatures, copies of records, and record retention. Each section provides points to evaluate like ensuring limited system access, time-stamped audit trails, unique electronic signatures, and the ability to produce accurate copies of electronic records. The document aims to help organizations evaluate their systems and processes to ensure compliance with FDA regulations for electronic records.
This document discusses various post-approval requirements and processes for pharmaceutical drugs, including prior approval supplements, changes being effected in 30 days supplements, annual reports, labeling changes, recalls, FDA inspections, and ISO 31000 risk management standards. It provides details on submission requirements and timelines for different types of post-approval changes, as well as FDA enforcement actions like warning letters, seizures, and injunctions.
The document provides information on documentation practices in the pharmaceutical industry. It discusses why documentation is important, defining documentation as written evidence of activities. It states that regulatory bodies prioritize reviewing documents to verify activities. Good documentation practices, including systematic preparation and review of documents, are required to prevent errors and ensure compliance. Documentation provides records, traceability, and audit trails for investigation and review.
The document discusses post-approval changes that can be made to approved NDAs and ANDAs. It describes four reporting categories for post-approval changes based on their potential impact: major changes requiring prior approval, moderate changes reported via a CBE-30 or CBE-0 supplement, minor changes reported annually. Examples are provided for different types of changes that fall under each reporting category. The levels of reporting ensure that manufacturers can make certain changes while providing appropriate notification to the FDA depending on the level of change.
This document discusses Good Automated Laboratory Practices (GALP) which provide guidance for managing automated regulated laboratories. It outlines the importance of standard operating procedures, documentation, logs, training, and concludes that GALP helps streamline laboratory processes and ensures work can be done efficiently within shorter timeframes. Key aspects of GALP covered include security, data management, error handling, change control, archiving, backup and recovery, and hardware maintenance.
REGULATORY REQUIREMENTS FOR ASEAN COUNTRIESVikas Rathee
The document discusses regulatory requirements for drug registration in Asian countries. It provides an overview of the ASEAN Common Technical Dossier (ACTD) format for drug applications across ASEAN countries. It then summarizes requirements for registration in China, South Korea, and with the ASEAN region. For China, it outlines the drug classification system and two-step approval process. For South Korea, it describes the drug classification and approval process including investigational new drug applications. It also provides background on the goals and formation of the ASEAN economic alliance between Southeast Asian countries.
The document defines FDA warning letters and describes the process of FDA inspections that can lead to warning letters. It explains that warning letters notify companies of violations found during inspections and investigations. Companies must promptly correct issues and FDA will check that corrections are adequate. The document also describes different types of warning letters for various regulated industries and how to browse existing warning letters on the FDA website.
This document provides an overview of FDA regulations 21 CFR Parts 210 and 211, which establish current Good Manufacturing Practices (cGMP) for manufacturing, processing, packing, or holding of drugs.
The summary includes definitions of key terms such as batch, component, drug product, and quality control. It also summarizes some of the major requirements for facilities, equipment, components, containers and closures, organization and personnel, and production and process controls to ensure identity, strength, quality and purity of drug products. The goal of Parts 210 and 211 is to provide minimum requirements and requirements for quality systems, not prescribe specific ways to meet those requirements.
The document discusses New Drug Applications (NDAs) submitted to the FDA for approval of new drug products. It describes how NDAs contain data from animal and human clinical trials demonstrating a drug's safety and effectiveness. There are different types of NDAs depending on if a drug is novel or similar to existing drugs. The FDA reviews NDAs to determine if manufacturing is adequate and if a drug's benefits outweigh its risks based on the application contents and recommendations are made for approval or further work required. Approved drugs require ongoing safety monitoring and reporting to the FDA.
The document outlines good manufacturing practices (GMP) for nutraceuticals. It discusses 12 key areas that GMP for nutraceuticals covers: 1) Premises, 2) Equipment, 3) Personnel, 4) Quality Assurance, 5) Sanitation Program, 6) Operations, 7) Specifications, 8) Stability, 9) Samples, 10) Records, and 11) Recalls. Under each area, it provides details on requirements. For premises, it describes requirements for personnel and material flow, walls/ceilings, HVAC systems, utilities, and pest control. It emphasizes the need for preventative maintenance of equipment, calibration of instruments, and cleaning procedures. It also outlines personnel requirements for
This document describes a case study on implementing change control for a Brookfield viscometer that was experiencing frequent spindle speed changes without human handling. This was affecting manufacturing processes and resulting in misleading viscosity readings. A change control process was initiated to address calibration intervals and validation procedures for the viscometer. Documentation was created justifying the need for the change and submitted to the quality assurance team for review and approval. Once approved, the change was implemented.
The document discusses guidelines for Active Substance Master Files (ASMF) and European Drug Master Files (EDMF) in the European Union. Some key points:
- An ASMF/EDMF contains quality and quality control information for an active pharmaceutical ingredient. It has two parts - an applicant part given to marketing authorization applicants, and a restricted part for regulatory authorities.
- The ASMF procedure can be used for new active substances, existing substances not in pharmacopeias, and pharmacopeial substances. It cannot be used for biological substances.
- Marketing authorization applicants must include specified information from the ASMF in their application dossier and have access to the current active substance manufacturer. ASMF
International Medical Device Regulators ForumSanthiNori1
The document summarizes the International Medical Device Regulators Forum (IMDRF), which was established in 2011 to accelerate international harmonization of medical device regulations. It provides background on IMDRF's establishment and membership, which includes regulators from 11 countries and regions. The document also discusses IMDRF's relationship to the prior Global Harmonization Task Force (GHTF) and describes IMDRF's management structure, meetings, and current working groups on issues like adverse event terminology and medical device cybersecurity.
Documentation in Pharmaceutical Industry Part I Tarif Hussian
This document discusses documentation practices in the pharmaceutical industry. It provides definitions of key terms like documentation and good documentation practices. It also describes important pharmaceutical documents like those related to drug substance, drug product, and exploratory product development briefs. These documents provide information on development, manufacturing, testing, and controls of drugs to ensure their quality, safety and efficacy. Adherence to documentation standards like ALCOA and ALCOA+ helps ensure the integrity and reliability of data in the pharmaceutical industry.
Presentation at ACI Conference on FDA Enforcement, covered:
Warning Letters, FDA Case Referral Process/Role of DOJ and U.S. Attorney, Coordination with States, Collateral Consequences of FDA Enforcement Actions
The document discusses batch production record (BPR) review and release. It defines key terms like deviations, critical process parameters, critical quality attributes. It outlines regulatory requirements from ICH Q7, CFR 211, and consequences of non-compliance. The objectives of BPR review are to confirm the batch quality and was produced under control. Records of critical steps must be reviewed and approved by quality before release. Failure to comply with cGMPs can render a drug adulterated under the FDA act.
Product lifecycle management: process of managing the entire lifecycle of a product from its conception, through design and manufacture, to service and disposal.
The document discusses the inspection of drug distribution channels. It covers the qualifications and attributes of drug inspectors, which include good knowledge of pharmacy laws and regulations, as well as integrity and communication skills. It also describes the organizational aspects of inspectors and different methods of inspection, such as comprehensive, concise, follow-up, and investigative inspections. The objectives of inspecting establishments are to ensure protection of patients, high ethical standards, and compliance with regulations. Special categories of drugs may require a modified inspection procedure.
STUDIES IN SUPPORT OF SPECIAL POPULATIONS : GERIATRICSMegha bhise
This document discusses guidelines for studies supporting the use of drugs in geriatric populations. It recommends including meaningful numbers of geriatric patients in Phase 3 clinical trials to compare drug responses between older and younger patients. Pharmacokinetic studies are important to determine if a drug's behavior differs in elderly subjects, such as due to changes in renal or hepatic function. Drug-drug interaction studies are also recommended to account for polypharmacy in geriatric patients.
The document outlines regulations regarding informed consent for biomedical research involving human subjects. It states that informed consent must be obtained from all research participants or their legal guardians. Informed consent documents must include key information such as the study's purpose and procedures, risks and discomforts, benefits, confidentiality protections, and participants' rights to withdraw. Researchers have obligations to fully inform participants and respect their autonomy by ensuring participation is voluntary and without coercion. Special procedures are required for vulnerable populations like children.
Flevy.com - Feasibility Study Template for Electronic Software DistributionDavid Tracy
This is a partial preview of the document found here:
https://flevy.com/browse/business-document/electronic-software-distribution-feasibility-study-32
Description:
This is a template to conduct a paper-based feasibility study to identify an Electronic Software Distribution tool or service.
Object-oriented programming uses abstraction and encapsulation through abstract data types (ADTs). An ADT defines a data type and its interface independently of its implementation. This allows information hiding and modular program design. Common languages like C++, Java, and Ruby support ADTs through classes or modules, which package data with methods, support inheritance and polymorphism, and provide visibility control through private/public access specifiers. Parameterized ADTs allow a data type to work with different element types. Namespaces and packages provide separate scopes to avoid naming conflicts.
The document provides information on documentation practices in the pharmaceutical industry. It discusses why documentation is important, defining documentation as written evidence of activities. It states that regulatory bodies prioritize reviewing documents to verify activities. Good documentation practices, including systematic preparation and review of documents, are required to prevent errors and ensure compliance. Documentation provides records, traceability, and audit trails for investigation and review.
The document discusses post-approval changes that can be made to approved NDAs and ANDAs. It describes four reporting categories for post-approval changes based on their potential impact: major changes requiring prior approval, moderate changes reported via a CBE-30 or CBE-0 supplement, minor changes reported annually. Examples are provided for different types of changes that fall under each reporting category. The levels of reporting ensure that manufacturers can make certain changes while providing appropriate notification to the FDA depending on the level of change.
This document discusses Good Automated Laboratory Practices (GALP) which provide guidance for managing automated regulated laboratories. It outlines the importance of standard operating procedures, documentation, logs, training, and concludes that GALP helps streamline laboratory processes and ensures work can be done efficiently within shorter timeframes. Key aspects of GALP covered include security, data management, error handling, change control, archiving, backup and recovery, and hardware maintenance.
REGULATORY REQUIREMENTS FOR ASEAN COUNTRIESVikas Rathee
The document discusses regulatory requirements for drug registration in Asian countries. It provides an overview of the ASEAN Common Technical Dossier (ACTD) format for drug applications across ASEAN countries. It then summarizes requirements for registration in China, South Korea, and with the ASEAN region. For China, it outlines the drug classification system and two-step approval process. For South Korea, it describes the drug classification and approval process including investigational new drug applications. It also provides background on the goals and formation of the ASEAN economic alliance between Southeast Asian countries.
The document defines FDA warning letters and describes the process of FDA inspections that can lead to warning letters. It explains that warning letters notify companies of violations found during inspections and investigations. Companies must promptly correct issues and FDA will check that corrections are adequate. The document also describes different types of warning letters for various regulated industries and how to browse existing warning letters on the FDA website.
This document provides an overview of FDA regulations 21 CFR Parts 210 and 211, which establish current Good Manufacturing Practices (cGMP) for manufacturing, processing, packing, or holding of drugs.
The summary includes definitions of key terms such as batch, component, drug product, and quality control. It also summarizes some of the major requirements for facilities, equipment, components, containers and closures, organization and personnel, and production and process controls to ensure identity, strength, quality and purity of drug products. The goal of Parts 210 and 211 is to provide minimum requirements and requirements for quality systems, not prescribe specific ways to meet those requirements.
The document discusses New Drug Applications (NDAs) submitted to the FDA for approval of new drug products. It describes how NDAs contain data from animal and human clinical trials demonstrating a drug's safety and effectiveness. There are different types of NDAs depending on if a drug is novel or similar to existing drugs. The FDA reviews NDAs to determine if manufacturing is adequate and if a drug's benefits outweigh its risks based on the application contents and recommendations are made for approval or further work required. Approved drugs require ongoing safety monitoring and reporting to the FDA.
The document outlines good manufacturing practices (GMP) for nutraceuticals. It discusses 12 key areas that GMP for nutraceuticals covers: 1) Premises, 2) Equipment, 3) Personnel, 4) Quality Assurance, 5) Sanitation Program, 6) Operations, 7) Specifications, 8) Stability, 9) Samples, 10) Records, and 11) Recalls. Under each area, it provides details on requirements. For premises, it describes requirements for personnel and material flow, walls/ceilings, HVAC systems, utilities, and pest control. It emphasizes the need for preventative maintenance of equipment, calibration of instruments, and cleaning procedures. It also outlines personnel requirements for
This document describes a case study on implementing change control for a Brookfield viscometer that was experiencing frequent spindle speed changes without human handling. This was affecting manufacturing processes and resulting in misleading viscosity readings. A change control process was initiated to address calibration intervals and validation procedures for the viscometer. Documentation was created justifying the need for the change and submitted to the quality assurance team for review and approval. Once approved, the change was implemented.
The document discusses guidelines for Active Substance Master Files (ASMF) and European Drug Master Files (EDMF) in the European Union. Some key points:
- An ASMF/EDMF contains quality and quality control information for an active pharmaceutical ingredient. It has two parts - an applicant part given to marketing authorization applicants, and a restricted part for regulatory authorities.
- The ASMF procedure can be used for new active substances, existing substances not in pharmacopeias, and pharmacopeial substances. It cannot be used for biological substances.
- Marketing authorization applicants must include specified information from the ASMF in their application dossier and have access to the current active substance manufacturer. ASMF
International Medical Device Regulators ForumSanthiNori1
The document summarizes the International Medical Device Regulators Forum (IMDRF), which was established in 2011 to accelerate international harmonization of medical device regulations. It provides background on IMDRF's establishment and membership, which includes regulators from 11 countries and regions. The document also discusses IMDRF's relationship to the prior Global Harmonization Task Force (GHTF) and describes IMDRF's management structure, meetings, and current working groups on issues like adverse event terminology and medical device cybersecurity.
Documentation in Pharmaceutical Industry Part I Tarif Hussian
This document discusses documentation practices in the pharmaceutical industry. It provides definitions of key terms like documentation and good documentation practices. It also describes important pharmaceutical documents like those related to drug substance, drug product, and exploratory product development briefs. These documents provide information on development, manufacturing, testing, and controls of drugs to ensure their quality, safety and efficacy. Adherence to documentation standards like ALCOA and ALCOA+ helps ensure the integrity and reliability of data in the pharmaceutical industry.
Presentation at ACI Conference on FDA Enforcement, covered:
Warning Letters, FDA Case Referral Process/Role of DOJ and U.S. Attorney, Coordination with States, Collateral Consequences of FDA Enforcement Actions
The document discusses batch production record (BPR) review and release. It defines key terms like deviations, critical process parameters, critical quality attributes. It outlines regulatory requirements from ICH Q7, CFR 211, and consequences of non-compliance. The objectives of BPR review are to confirm the batch quality and was produced under control. Records of critical steps must be reviewed and approved by quality before release. Failure to comply with cGMPs can render a drug adulterated under the FDA act.
Product lifecycle management: process of managing the entire lifecycle of a product from its conception, through design and manufacture, to service and disposal.
The document discusses the inspection of drug distribution channels. It covers the qualifications and attributes of drug inspectors, which include good knowledge of pharmacy laws and regulations, as well as integrity and communication skills. It also describes the organizational aspects of inspectors and different methods of inspection, such as comprehensive, concise, follow-up, and investigative inspections. The objectives of inspecting establishments are to ensure protection of patients, high ethical standards, and compliance with regulations. Special categories of drugs may require a modified inspection procedure.
STUDIES IN SUPPORT OF SPECIAL POPULATIONS : GERIATRICSMegha bhise
This document discusses guidelines for studies supporting the use of drugs in geriatric populations. It recommends including meaningful numbers of geriatric patients in Phase 3 clinical trials to compare drug responses between older and younger patients. Pharmacokinetic studies are important to determine if a drug's behavior differs in elderly subjects, such as due to changes in renal or hepatic function. Drug-drug interaction studies are also recommended to account for polypharmacy in geriatric patients.
The document outlines regulations regarding informed consent for biomedical research involving human subjects. It states that informed consent must be obtained from all research participants or their legal guardians. Informed consent documents must include key information such as the study's purpose and procedures, risks and discomforts, benefits, confidentiality protections, and participants' rights to withdraw. Researchers have obligations to fully inform participants and respect their autonomy by ensuring participation is voluntary and without coercion. Special procedures are required for vulnerable populations like children.
Flevy.com - Feasibility Study Template for Electronic Software DistributionDavid Tracy
This is a partial preview of the document found here:
https://flevy.com/browse/business-document/electronic-software-distribution-feasibility-study-32
Description:
This is a template to conduct a paper-based feasibility study to identify an Electronic Software Distribution tool or service.
Object-oriented programming uses abstraction and encapsulation through abstract data types (ADTs). An ADT defines a data type and its interface independently of its implementation. This allows information hiding and modular program design. Common languages like C++, Java, and Ruby support ADTs through classes or modules, which package data with methods, support inheritance and polymorphism, and provide visibility control through private/public access specifiers. Parameterized ADTs allow a data type to work with different element types. Namespaces and packages provide separate scopes to avoid naming conflicts.
This document provides an overview of object-oriented programming concepts including classes, objects, inheritance, encapsulation, polymorphism and abstraction. It discusses SOLID principles like single responsibility, open/closed, Liskov substitution, interface segregation and dependency inversion. It also covers UML diagrams, architecture styles and data access layers.
A Security hole in an application can cause not only major financial loss but also loss of customer confidence, trust and reputation severely impacting the business. This webinar looks at well-established industry practices to identify and secure applications from breaches while adhering with regulatory compliances.
FixNix aims to develop a GRC Suite leveraging latest technologies. Their GRC Suite would comprise modules for audit management, risk management, asset management, policy management, security incident management, compliance management, fraud management, business continuity management, vendor management, and contract management. It aims to provide customizable, configurable, and easy to use tools to automate GRC processes and provide integrated dashboards and reporting across all modules.
Information technology has significantly impacted the accounting discipline by introducing new ways to retrieve and process performance and control information. IT systems like ERP separate financial from non-financial data, enabling better accounting. However, they also provide new potential for management control as data becomes more shareable. Information system auditing evaluates information systems to assess control effectiveness and adequacy in helping an organization achieve its objectives. It identifies risks from IT usage and suggests control improvements. Key elements of IS audits include assessing data, applications, technology, facilities, people, and reviewing system administration, software, network security, business continuity, and data integrity.
The document describes jComply, a governance, risk and compliance software platform. It allows users to manage policies and procedures, perform risk assessments, ensure compliance and audit functions, track incidents and accidents, and provide training. The platform integrates various modules to help companies improve performance, reduce costs, and develop a positive compliance culture while achieving regulatory requirements.
The document discusses Expertool's GRC Acceleration solution which helps companies more quickly implement and update governance, risk, and compliance (GRC) systems. It does this by optimizing required human tasks, defining automation requirements, and supporting GRC content governance. The solution provides deliverables like analyzing GRC architecture and content, prototyping business rules, and establishing a content governance environment to reduce the time and effort of GRC system implementation and maintenance.
FulcrumWay - Ed. Webinar - Identify and Eliminate False Positives from your S...FulcrumWay
This Education Webinar presentation was to learn to Identify and Eliminate False Positives from your Segregation of Duty Audit Report. Segregation of Duties (SOD) controls over business transactions and sensitive data provide an effective safeguard against financial misstatement risks, fraud and operational losses. Big-4 Audit Firms include SOD testing in their audit plan, as well as many organizations have invested in internal SOD tools to provide continuous monitoring of application access controls. However, SOD Audit Reports contain many False Positive issues that can bog down ERP Applications, Finance and Internal Audit teams. Therefore, identifying and eliminating False Positives is a key step in the SOD risk management approach. In this educational webinar you will learn how to identify false positives that are generated due to the complexity of the Oracle EBS security model. We will provide a checklist of “known” False Positives as well as provide you an approach to identify “unknown” False Positives resulting from overriding securing attributes; for example, a “Buyer” Profile Option is required to Create Purchase Order entitlements in Oracle EBS. You will learn the latest techniques to eliminate False Positive violations using “filters” in the SOD tool and reports based on our recent client case studies. We will also share some examples of SOD Analytics Reports that can help you track your SOD Remediation Plan after you remove the False Positives. Introduction • Inherent False Positives in Oracle EBS Security Model • Checklist of Global False Positives • Systematic Approach for Identifying False Positives • SOD Analytics for Remediation Analysis • Case Study • Q&A Join us for this webinar if your role and responsibilities include: • Chief Security Officers • System Administrators • Oracle EBS Consultants • Oracle GRC Advanced Controls Administrator • Compliance (SOX) & Control Manager • Internal Auditors & External Auditors Our ERP advisors have 20+ years of experience in Oracle EBS, System Audits, SOX Compliance, Oracle GRC Implementations & IT Governance at Big-4, Oracle and/or NYSE/NASDAQ public co.
The presentation sheds light on the concept of GRC (Governance, Risk and Compliance). Features associated to GRC, such as - its history, its impact on businesses, types etc are covered here.
Here is the list of the topics covered:
1. How was GRC developed?
2. What exactly is GRC?
3. The role of GRC in ISMS
4. Impact of GRC
5. Types of GRC
6. The role IT-GRC in IT-RMC
7. IT-GRC Foundation
8. Why to deploy IT-GRC Management System?
This document provides a company profile for DFLabs, an ISO-certified cybersecurity firm. DFLabs specializes in information security governance, risk, and compliance. The company provides IT risk management frameworks, incident response services, digital forensics, and security consulting. DFLabs operates globally from headquarters in Northern Italy and has Fortune 100 customers. The company focuses on closing the gap between growing security risks and organizations' capacity to respond through an integrated IT governance framework.
Anna is a college senior searching for a job in New York City. Living in the expensive city will be difficult once her parents stop providing money after graduation. She sees an ad for a job downtown that sounds interesting and pays well. Her college counselor tells her she needs to fill out an application, write a resume, and include a cover letter. Anna completes the application materials and sends them in. She receives a call inviting her to an interview, which goes well. The next day, she is offered the job.
The document provides a list of 14 discussion topics across various categories including dating, fashion, food, movies, music, sports, travel, nightlife, news, language learning, and the internet. For each topic, there are 2-4 questions provided, and participants are asked to choose 3 topics to draft responses for each question in that topic. They are also asked to generate their own additional question for each of the 3 topics they choose.
Mosquitoes find humans using carbon dioxide, warmth, and movement. Female mosquitoes require blood meals to develop their eggs. There are four stages in a mosquito's lifecycle - egg, larva, pupa, and adult. Mosquitoes lay their eggs in various standing waters, where the larvae live until becoming pupae and then emerging as adult mosquitoes. Their tiny wing scales help them fly efficiently and make swatting difficult.
Course Outline Materials Development and AdaptationSalina Saharudin
1) This course outline provides information on a 3 credit course called Materials Development and Adaptation offered through the Department of English at a university.
2) The course aims to evaluate current English language teaching materials used in schools, teach criteria for materials evaluation, and discuss techniques for developing and adapting materials.
3) Assessment includes assignments evaluating and developing original teaching materials, tests, and a portfolio compiling all coursework materials.
The document discusses identifying verbs and adverbs in writing. It defines verbs as words that indicate action and identifies the main types of verbs including helping verbs, verb phrases, modal verbs, and forms of the verb "to be." It also discusses identifying adverbs and their function in modifying verbs, adjectives, and other adverbs. The document concludes with an exercise identifying verbs, verb phrases, and other parts of speech in sample sentences.
This document provides examples of subject-verb agreement errors and exercises for students to identify the correct verb form based on the subject. There are 3 sections: A) sentences where the subject and verb must agree are underlined, B) the correct verb form is underlined from options in parentheses, and C) the correct verb form is underlined when substituting pronouns for nouns as subjects. The document aims to help students learn and practice subject-verb agreement.
The document provides an overview of the impact of emerging technologies on the American educational system in the late 1990s and early 2000s. It discusses how technologies like computers, internet access, and digital resources rapidly proliferated in schools during this period. However, it also notes that the educational system struggled to adapt to this "information chaos" and that technologies were sometimes adopted more for marketing purposes than improving instruction. The document explores issues around balancing educational quality versus quantity and approaches versus avoidances of new technologies in this transitional period.
This document outlines the course details for CPD 2113 TECHNOLOGY IN ELT, including administrative information, learning objectives, course content, assessment tasks, and schedule. The 3-credit course aims to provide knowledge on using technology in education. Over 14 weeks, topics will include the role of technology, software/applications, and developing lesson plans and multimedia software. Assessment includes a group presentation evaluating educational software (20%), a final exam (20%), and a group multimedia software project with presentation and report (40%). The course is intended to help students understand and apply technology in their teaching.
This document is a subject-verb agreement exercise that contains:
1) 20 sentences with blanks to fill in the correct verb form based on the subject. Students are asked to underline the correct verb form.
2) An additional 21 sentences with blanks to fill in the correct verb based on whether the subject is singular or plural. Students are again asked to underline the correct verb form.
3) The purpose is to practice identifying subjects and choosing the appropriate verb to maintain subject-verb agreement in sentences.
Agrarian vs. hunter gatherer website rubric - unit 2Scott Marsden
The rubric evaluates websites about agrarian vs. hunter-gatherer societies on several criteria including required content, written communication, oral communication, technology, and collaboration. The criteria are rated on a scale from unsatisfactory to advanced. Required content addresses key topics such as the origins of agriculture and cities and is to be appropriate for a 6th grade audience. Written communication considers spelling, grammar, diction, and paragraph organization. Oral communication evaluates volume, delivery, memorization and professionalism. Technology examines navigation, layout, consistency and functionality. Collaboration focuses on equal participation and task focus during group work.
Agrarian vs. hunter gatherer website rubric - unit 2Scott Marsden
The rubric evaluates websites about agrarian vs. hunter-gatherer societies on several criteria including required content, written communication, oral communication, technology, and collaboration. The criteria are rated on a scale from unsatisfactory to advanced. Required content addresses key topics such as the origins of agriculture and cities and is to be appropriate for a 6th grade audience. Written communication considers spelling, grammar, diction, and paragraph organization. Oral communication evaluates volume, delivery, memorization and professionalism. Technology examines navigation, layout, consistency and functionality. Collaboration focuses on equal participation and task focus during group work.
The Six Traits Writing Rubric provides a scale to evaluate student writing across six traits: Ideas & Content, Organization, Voice, Word Choice, Sentence Fluency, and Conventions. For each trait, the rubric describes the characteristics of writing that would be considered Exemplary (6), Strong (5), Proficient (4), Developing (3), Emerging (2), or Beginning (1).
This document provides strategies for developing writing skills in students. It discusses managing the writing workshop with large blocks of time, modeling writing, practicing specific criteria, and using formative assessment. Key aspects of the writing traits like ideas, organization, voice, word choice, sentence fluency, and conventions are defined. Strategies like quick writes, building criteria with students, and using artifacts to inspire story writing are presented.
This document provides a rubric to evaluate student participation in classroom discussions. It evaluates students in three key areas: participation in classroom discussion, respect for peers, and behavior. For each area, it provides criteria for ratings of excellent, satisfactory, fair, and needs improvement. For participation, it evaluates how often a student actively engages in discussions. For respect, it evaluates listening skills and treatment of peers. For behavior, it evaluates how well a student follows classroom rules and stays on task. The rubric provides clear guidelines for teachers to assess student participation and engagement in classroom discussions.
This rubric evaluates documents on content, graphics and layout, and criteria for excellent, very good, satisfactory, and needs improvement work. For content, excellent work has clear objectives and accurate information, complete citations, and ideas are fully summarized. Graphics and layout are excellent if fonts and visuals enhance readability and content, with smooth transitions between sections and an effective layout. Work needs improvement if objectives are unclear, information is missing or inaccurate, citations are incomplete, or ideas are not well summarized.
This document provides tips for success in online programs. It emphasizes establishing a dedicated study space at home, managing time effectively by setting deadlines and goals, using proper equipment like a reliable computer and headset, communicating regularly via email and course sites, understanding instructor expectations, and maintaining proper online communication etiquette. The overall message is that with the right preparation and organization, online learning can be a positive experience.
Preparing staff and volunteers for working with the dementia population handoutsStephenVozzellaSlides
This presentation provides tools for training staff and volunteers on working with the dementia population. The presenter discusses different learning styles, topics to cover in training programs, and techniques for leading effective presentations. The objectives are to describe learner types, identify successful teaching methods, and implement a basic volunteer training program. Examples are given for training content, lesson plans, and leading interactive sessions. Emphasis is placed on practical skills like communication, documentation, and understanding dementia types and symptoms.
The document provides information about an online teaching institute summer session in 2011, including frequently asked questions. It addresses questions about the time commitment required, expectations for online etiquette, how assignments will be submitted, and whether students need their own computer or can access courses online. The summary emphasizes that online courses require self-motivation, good time management and computer skills, have firm deadlines, and expect professional communication and academic honesty.
This document provides frequently asked questions (FAQ) for an online course. It addresses questions about student characteristics, online etiquette, course structure, assignments, communication tools, and technical requirements. Key details include emphasizing self-motivation, time management, and academic honesty. Communication will occur through email, discussion boards, and virtual office hours. Students should expect the same workload as a face-to-face class. No prior online experience or computer ownership is required, though basic computer skills are helpful.
This document provides an overview of a presentation for parents on digital literacy and parenting in the digital age. It discusses digital life and literacy, technology used for learning at NIS including MacBooks, iWork, wikis and iCal. It covers tips for parents on social networks, online gaming, creating secure passwords and balancing digital and non-digital activities. It also advertises a workshop on creating podcasts.
This document provides a guide for parents on assessment and grading practices for 4th grade. It outlines the Common Core standards for English/Language Arts, Math, Social Studies and Science. It also includes samples of progress reports and rubrics used to evaluate student work. The document discusses a shift from traditional grading to mastery-based learning where students can improve work until they demonstrate understanding. Homework and late/incomplete work policies are explained. The teacher's goals are to help all students master content and become lifelong learners through meaningful learning experiences and open communication.
The document summarizes revisions to the rating rubric for the ECPE writing test that will take effect in June 2009. A new level "E" will be added below the existing level "D" to provide more granularity in scoring. The descriptors for levels A through C will remain the same, but level D will be divided into a new level D and the new lowest level E. The minimum passing score will remain a C. The writing task itself will not change.
This document provides a scoring rubric for presentations with 5 traits being scored on a scale of 1 to 5. The 5 traits are: Information Quality and Organization, Nonverbal Communication, Quality of Verbal Communication, Visual Tools, and Precision and Detail in Documents Produced. Each trait has descriptors for what a score of 1, 3, or 5 would entail. An additional trait of Overall Presentation Effectiveness is included and also scored on a 1 to 10 scale. The rubric aims to provide an objective means of evaluating presentations across several key areas.
This document provides guidance on making effective presentations. It discusses four key stages: thinking about the context and content, structuring the presentation, writing a draft, and practicing and reviewing. The context includes the audience, their background and understanding, and the environment. The content focuses on main points to discuss and supporting information. An effective structure builds upon three main points with an introduction and summary. With careful planning and practice, presentations can be successful.
This document outlines the tasks, process, and evaluation for a student project to design a city on another planet. Students will be divided into groups to research planets, design livable cities, plan activities and jobs, address environmental factors, and present their designs. They will use suggested online resources and cite any non-original work. Groups will be evaluated on organization, detail, mechanics, internet use, and diagrams/illustrations. The goal is for students to successfully create hypothetical off-world colonies and communities.
This document provides guidance on effective PowerPoint presentations. It discusses advantages like employing visual aids and incorporating different media. Disadvantages include presentations dominating over speaker ideas. Proper planning is important, including understanding why, how, when to use PowerPoint. Formatting tips include using limited colors, readable text sizes, and simple graphs. Speakers should enhance but not replace their ideas. Effective listeners focus on messages over styles.
This document provides tips for delivering effective presentations to stakeholders. It recommends knowing your subject matter, audience, and yourself. The presenter should develop a clear theme and script. Visual aids should support the content, not distract, using plain fonts, bullet points, and consistent backgrounds. Rehearsing is key to timing, comfort with the materials, and soliciting feedback. The overall goals are to communicate the essential information simply, clearly, and engagingly.
The document introduces both hard skills like programming and design skills as well as soft skills needed by engineers, discussing categories of soft skills including corporate skills, employability skills, and life skills. It then provides details on developing key soft skills like communication, presentation, and language skills through practices like reading, writing, speaking, listening, and incorporating visual elements into presentations.
The Science of Visual Design: Creating Strong Graphics for IDJames Washok
As an instructional designer with a background in graphic design, I see a lot of poorly created materials due to the lack of an understanding of the of the SCIENCE behind visuals.
Technical English 2 (May 2015) - Reading MaterialSalina Saharudin
This text discusses the principle that individuals should only be compelled or controlled by society through force or social pressure to prevent harm to others, not for their own benefit. It asserts that an individual's liberty can only rightfully be interfered with for self-protection purposes. The only justification for exercising power over someone against their will is to prevent harm to others, as their own good is not a sufficient reason to compel them to act in a certain way or restrain them.
This document outlines the syllabus for a Technical English II course offered at the Centre of Foundation and General Studies. The course is worth 3 credit hours and will focus on developing students' academic English skills as well as introducing occupational components to prepare them for future studies and jobs. Assessment will include two online tests, assignments, presentations, and a final exam. The lecturer is Murni Salina and the course objectives are to equip students with language skills for effective social, business, and workplace communication and to develop their ability to understand and respond critically to texts and write accurately for academic and occupational purposes. The course schedule provides details of topics to be covered in each of the 14 lectures, including strategies for reading, writing, speaking, grammar
This document is a textbook evaluation tool that consists of 6 parts for reviewing textbooks. It includes sections to rate the organization/format, content, teacher's edition/supplementary materials, inclusion/equity/diversity issues, and alignment with district curriculum and state standards of the textbook. Reviewers are asked to rate various criteria on a scale from 0 to 3 to evaluate different aspects of the textbook.
This document discusses evaluation criteria for English language teaching materials from several studies and sources:
- Rahimpour & Hashemi (2011) evaluate content, physical make-up, and practical concerns. Jayakaran & Nimechisalem (2011) consider compatibility with teaching principles and balance of language skills.
- Tsiplakides (2011) evaluate how tasks contribute to language acquisition and development and how activities progress and vary.
- Inal (2006) lists 11 criteria including relevance of subjects/contents and language, interest, variety, authenticity, and cultural sensitivities.
- Robinett (1978) cited in Yilmaz (2005) considers goals, students, approaches
This document discusses different types of textbook evaluation:
- Pre-use evaluation assesses potential without experience using the book. It examines potential performance.
- In-use evaluation occurs while materials are being used, to monitor newly introduced or aging books. It assesses suitability.
- Post-use evaluation retrospectively assesses performance of books already used, to decide whether to continue use. It also assesses suitability.
External evaluation examines claims on the cover and introduction, as well as the table of contents to understand intended audience, level, context, and presentation. Internal evaluation investigates skills presentation, grading, practice opportunities, authenticity, tests, and motivation factors. The overall evaluation considers usability, general
This document discusses different types of textbook evaluation:
- Pre-use evaluation occurs before a book is used and examines potential performance.
- In-use evaluation happens while a book is being used to monitor newly introduced or aging materials.
- Post-use evaluation provides a retrospective assessment of a book's performance after it has been used.
It also outlines factors to consider for external evaluation of a book's description and claims, and internal evaluation of how language skills, materials, and tests are presented. The overall evaluation examines a book's usability, general features, adaptability, and flexibility.
The document discusses the process and approaches for evaluating instructional materials. It describes the selection process as having 7 steps: 1) identifying program aims and objectives, 2) analyzing the teaching and learning situation, 3) finding or designing an evaluation checklist, 4) limiting criteria, 5) creating a shortlist, 6) in-depth evaluation using the checklist, and 7) making a selection decision. It also outlines two main evaluation approaches - impressionistic overview and in-depth evaluation, and notes that combining both forms a sound evaluation basis. Several evaluation methods are mentioned, including piloting materials, gathering teacher and student opinions, and detailed analysis.
This document discusses materials evaluation in language learning. It defines materials evaluation as the systematic appraisal of instructional materials to measure their impact on language learning quality. Materials evaluation examines the potential and practicality of materials, and helps teachers determine if materials should be adopted, maintained, or replaced based on their strengths, weaknesses, and how well they meet learner and teacher needs. The document also outlines the purposes of materials evaluation such as adopting new textbooks, identifying issues with current materials, comparing options, and informing teacher training. Both predictive evaluation of potential future materials and retrospective evaluation of past materials use are discussed.
The document discusses the roles and advantages of instructional materials, particularly textbooks. Textbooks can serve as resources for teaching materials and activities, references for language skills, and supports for less experienced teachers. While textbooks provide structure and standardized lessons, they also have disadvantages like being inflexible and containing inauthentic language. Ideal textbook use supplements them with other materials to give teachers and students more flexibility.
Materials refer to anything used in language teaching and learning, including textbooks, CD-ROMs, DVDs, handouts, charts, and websites. Materials can be informative, instructional, experiential, or exploratory. Commercially produced materials mostly focus on informing learners about language features and guiding practice. Material development involves evaluating, adapting, designing, producing, and researching materials for language learning.
This document defines materials in language learning as textbooks, course books, CD-ROMs, DVDs, handouts, charts, and websites that teachers and learners use to teach and learn language. Materials can be informative, instructional, experiential, or exploratory, and commercially produced materials mostly focus on informing learners about language features and guiding practice. The development of materials involves evaluating, adapting, designing, producing, and researching materials to make language learning effective.
This document discusses the key components of a computer system. It identifies the main components as hardware, software, and warmware. A computer system performs four main tasks: receiving input, storing information, processing data, and outputting information. The document then examines the components that facilitate these tasks in more detail, including input devices, the processor, output devices, and storage. It provides examples of common input, processing, output, and storage devices and their functions.
An information system has five key components: people, procedures, software, hardware, and data. The document explains each component in detail - people are end-users, procedures are rules for using the system, software are computer programs, hardware are physical devices, and data is raw unprocessed information. An information system brings together these five elements to convert data into useful information for people.
Course Outline - Materials Development & AdaptationSalina Saharudin
This document outlines a course on materials development and adaptation for teaching English as a second language. The 3-credit course is offered through the Department of English at a Malaysian university. Key elements of the course include evaluating existing teaching materials based on established criteria, adapting materials to suit different student groups and skills, and developing original instructional materials. Assessment consists of evaluating an existing textbook, creating and presenting adapted materials, tests, and compiling a portfolio of class materials. The goal is for students to learn skills in appraising, selecting, adapting and developing materials to effectively teach English.
This article describes the development of an English language textbook evaluation checklist. The researchers first reviewed existing textbook evaluation checklists and identified common criteria. They then developed a tentative checklist organized into two main categories: general attributes and learning-teaching content. The general attributes section includes subcategories like relation to syllabus, methodology, suitability to learners, and physical attributes. The learning-teaching content section includes criteria for areas like listening, speaking, reading, writing, vocabulary and grammar. The researchers considered issues of validity, reliability and practicality in developing the checklist. They intend to further refine the checklist through additional research studies. The checklist is intended to help educators evaluate and select textbooks.
Charles Hanson and his wife got scared while camping in a Florida state park late one night. They realized the park was too isolated and dark for what they wanted. Many visitors leave parks at night due to getting scared. Different parks in Florida have varying levels of isolation, amenities, and types of environments that appeal to different kinds of visitors.
The document discusses what constitutes good essay writing. It notes that good essays (1) support ideas with evidence from references and related materials, (2) arrange complex ideas clearly without repetition, and (3) begin with an engaging introduction using simple language and sentences. Additional tips for good writing include rechecking for errors, signifying important points, choosing an interesting topic you have knowledge about, using a clear structure and flow, and following recommended formatting. Factors like an uninteresting topic, lack of background knowledge, and not following a format can negatively impact an essay. Writers should prepare by outlining major points before drafting to effectively convey their ideas.
The document discusses the differences between writing and speech. Some key differences are: 1) Writing is usually permanent whereas speech can be corrected and changed as it is spoken. 2) Written language tends to be more complex with longer sentences and clauses, while spoken language has repetitions and interruptions. 3) Writers can use punctuation, layout and graphics while speech uses tone, volume and timing.
This document discusses different types of writing systems. It begins by dividing writing systems into two main types: alphabets and syllabaries. Alphabets represent consonants and vowels, while syllabaries represent syllables. The document then describes several subcategories of writing systems, including abjads/consonant alphabets, alphabets, syllabic alphabets/abugidas, syllabaries, semanto-phonetic writing systems, undeciphered writing systems, and other communication systems such as codes. Each category is explained with examples to illustrate the characteristics of the writing system.
The document describes the standard symbols used in flowcharts including terminal blocks, process blocks, decision points, documents, on-page connectors, direction of flow indicators, hyperlinks, annotations, and unit separators. Each symbol is defined with a brief description of its purpose in visually representing processes and workflows.
हिंदी वर्णमाला पीपीटी, hindi alphabet PPT presentation, hindi varnamala PPT, Hindi Varnamala pdf, हिंदी स्वर, हिंदी व्यंजन, sikhiye hindi varnmala, dr. mulla adam ali, hindi language and literature, hindi alphabet with drawing, hindi alphabet pdf, hindi varnamala for childrens, hindi language, hindi varnamala practice for kids, https://www.drmullaadamali.com
Executive Directors Chat Leveraging AI for Diversity, Equity, and InclusionTechSoup
Let’s explore the intersection of technology and equity in the final session of our DEI series. Discover how AI tools, like ChatGPT, can be used to support and enhance your nonprofit's DEI initiatives. Participants will gain insights into practical AI applications and get tips for leveraging technology to advance their DEI goals.
ISO/IEC 27001, ISO/IEC 42001, and GDPR: Best Practices for Implementation and...PECB
Denis is a dynamic and results-driven Chief Information Officer (CIO) with a distinguished career spanning information systems analysis and technical project management. With a proven track record of spearheading the design and delivery of cutting-edge Information Management solutions, he has consistently elevated business operations, streamlined reporting functions, and maximized process efficiency.
Certified as an ISO/IEC 27001: Information Security Management Systems (ISMS) Lead Implementer, Data Protection Officer, and Cyber Risks Analyst, Denis brings a heightened focus on data security, privacy, and cyber resilience to every endeavor.
His expertise extends across a diverse spectrum of reporting, database, and web development applications, underpinned by an exceptional grasp of data storage and virtualization technologies. His proficiency in application testing, database administration, and data cleansing ensures seamless execution of complex projects.
What sets Denis apart is his comprehensive understanding of Business and Systems Analysis technologies, honed through involvement in all phases of the Software Development Lifecycle (SDLC). From meticulous requirements gathering to precise analysis, innovative design, rigorous development, thorough testing, and successful implementation, he has consistently delivered exceptional results.
Throughout his career, he has taken on multifaceted roles, from leading technical project management teams to owning solutions that drive operational excellence. His conscientious and proactive approach is unwavering, whether he is working independently or collaboratively within a team. His ability to connect with colleagues on a personal level underscores his commitment to fostering a harmonious and productive workplace environment.
Date: May 29, 2024
Tags: Information Security, ISO/IEC 27001, ISO/IEC 42001, Artificial Intelligence, GDPR
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Strategies for Effective Upskilling is a presentation by Chinwendu Peace in a Your Skill Boost Masterclass organisation by the Excellence Foundation for South Sudan on 08th and 09th June 2024 from 1 PM to 3 PM on each day.
Main Java[All of the Base Concepts}.docxadhitya5119
This is part 1 of my Java Learning Journey. This Contains Custom methods, classes, constructors, packages, multithreading , try- catch block, finally block and more.
This presentation was provided by Steph Pollock of The American Psychological Association’s Journals Program, and Damita Snow, of The American Society of Civil Engineers (ASCE), for the initial session of NISO's 2024 Training Series "DEIA in the Scholarly Landscape." Session One: 'Setting Expectations: a DEIA Primer,' was held June 6, 2024.
How to Manage Your Lost Opportunities in Odoo 17 CRMCeline George
Odoo 17 CRM allows us to track why we lose sales opportunities with "Lost Reasons." This helps analyze our sales process and identify areas for improvement. Here's how to configure lost reasons in Odoo 17 CRM
বাংলাদেশের অর্থনৈতিক সমীক্ষা ২০২৪ [Bangladesh Economic Review 2024 Bangla.pdf] কম্পিউটার , ট্যাব ও স্মার্ট ফোন ভার্সন সহ সম্পূর্ণ বাংলা ই-বুক বা pdf বই " সুচিপত্র ...বুকমার্ক মেনু 🔖 ও হাইপার লিংক মেনু 📝👆 যুক্ত ..
আমাদের সবার জন্য খুব খুব গুরুত্বপূর্ণ একটি বই ..বিসিএস, ব্যাংক, ইউনিভার্সিটি ভর্তি ও যে কোন প্রতিযোগিতা মূলক পরীক্ষার জন্য এর খুব ইম্পরট্যান্ট একটি বিষয় ...তাছাড়া বাংলাদেশের সাম্প্রতিক যে কোন ডাটা বা তথ্য এই বইতে পাবেন ...
তাই একজন নাগরিক হিসাবে এই তথ্য গুলো আপনার জানা প্রয়োজন ...।
বিসিএস ও ব্যাংক এর লিখিত পরীক্ষা ...+এছাড়া মাধ্যমিক ও উচ্চমাধ্যমিকের স্টুডেন্টদের জন্য অনেক কাজে আসবে ...
1. Software Evaluation Rubric
Title: Grade Level:
Publisher/copyright date: Operating system(s):
Unsatisfactory - 1 Needs Improvement - 2 Good - 3 Exemplary - 4 SCOR
E
• Information is inaccurate, • Information is not always • Information is accurate and • Information is accurate,
incomplete or outdated accurate, complete or most is complete and current complete, and current
current
• Facts do not come from • Facts come from • Facts usually come from • Facts come from reliable
reliable sources or sources questionable sources reliable sources which are sources which are clearly
are not identified clearly identified identified
• Little or no overall context • Content is not related to • Content is usually related to • Content and context are
for information larger context larger context consistent with the theme
• Purpose is unclear • Content lacks sense of • General purpose is • All information relates to
(a)
purpose or central theme identified the stated purpose and
learning goals
• Content focuses entirely • Content focuses on • Content provides some • Content moves learners
on fundamental concepts, fundamental concepts and activities which encourage beyond the basics and
rote memory, or recitation of rarely engages students in higher levels of thinking; encourages higher levels of
facts; no provision for higher levels of thinking; students are frequently asked thinking; students are
moving students to higher students are rarely asked to to apply what they have engaged in applying what
levels of thinking by applying apply what they learn learned they learn
what is learned
• National and/or state • National and/or state • National and/or state • National and state
standards are not accessible standards are not located standards are sometimes standards are accessible
within the product and there within the product but some available and may be linked within the product and may
are no apparent links to the relation to standards is to lessons be easily linked to lessons
learning activities apparent
• No prerequisite • Lists some prerequisite • Outlines prerequisite • Lists all prerequisite skills
knowledge requirements are knowledge necessary for knowledge necessary for
(b)
given success success
• No real world examples • Uses some real world • Uses many real world • Uses all real world
are given examples to make the examples to make the examples to make the
instruction relevant for the instruction relevant for the instruction relevant for the
learner learner learner
• Complies with some • Complies with most • Complies with all subject
subject based guidelines subject based guidelines based guidelines
2. • Graphics are absent, • Graphics minimally • Graphics are intended to • Graphics are well
poorly placed, or fail to support learning assist learning designed and rendered to
assist learning enhance learning
• Background and text are • Background and text • Background and text are • Background and text are
not compatible and text is are frequently incompatible usually pleasing, compatible pleasing, compatible and
difficult to read and text is often difficult to and legible easy to read
read
• Graphics are • Graphics are not always • Most graphics are • Graphics are consistent,
inconsistent, inappropriate, consistent or appropriate consistent and appropriate in appropriate and designed to
(c)
and do not enhance learning design optimize learning
• Poor use of color • Colors are used • Colors are used in a • Colors are used in an
somewhat ineffectively somewhat effective way effective way
• Gratuitous animation • Animation rarely • Animation often • Animation always
with no relation to learning complements learning complements learning complements learning
goals
• Multimedia is • Multimedia seems • Multimedia is sometimes • Multimedia appears to be
superfluous and often gets unrelated to purpose and unrelated to purpose and directly related to stated
in the way of purpose and learning goals learning goals purpose and learning goals
learning goals
• Layout is confusing • Layout is not intuitive • Layout is clear but learners • Layout is clear and
sometimes need help to find intuitive; learners can
necessary features always find what they need
• Learners cannot • Layout is difficult to • learners can usually • It is easy to navigate
navigate through the navigate navigate through the through the information to
information to find what they information to find what they find necessary features
(d)
need need
• Layout is illogical and • Layout is frequently • Layout is logical in most • Layout is logical
unpredictable illogical cases, but sometimes
confusing
• Layout is inconsistent • Layout is frequently • Layout is frequently • Layout is consistent on all
inconsistent consistent, but occasionally pages
confusing
• Links do not work • Not all links work • Most links work properly • All links work properly
properly properly
• Specific browser needed • Pages work in only one • Most pages work in most • Pages work in most
(e)
to view pages, but no browser , but directions and browsers common browsers:
directions are available for links are provided so users Netscape and Internet
users to download can download appropriate Explorer
appropriate browser browser
3. • Multimedia resources do • Multimedia resources • Multimedia resources work • All multimedia resources
not work work some of the time most of the time work at all times
• Web site is often down or • Web site is unreliable or • Users are able to access • Users are able to access
unreliable; software software is hard to install web site or install software web site or install software
installation often results in properly with minimal effort with ease
aborted efforts or conflicts
• Clear and complete
directions are available for
access or installation
• Pictures and icons do not • Few pictures and icons • Most pictures and icons • Hyperlinks have ALT tags
have ALT tags have ALT tags have ALT tags for rollover to assist sight-
impaired learners
• Paragraphs and sections • Some paragraphs and • Most paragraphs and • Paragraphs and sections
have unclear and inaccurate sections have clear and sections have clear and have clear and accurate
informative headings accurate informative accurate informative headings informative headings
headings
• Clear and clean fonts are • Clear and clean fonts • Clear and clean fonts are • Clear and clean fonts are
(f)
not used are used consistently some used consistently most of the used consistently
of the time time
• Content is not culturally • Some content is • Content includes some • Content is culturally
diverse culturally diverse culturally diverse features diverse
• Content does not • Some content • Most content • Product accommodates
accommodate unique accommodates unique accommodates unique unique learning styles and
learning styles and various learning styles and various learning styles and various various ability levels
ability levels ability levels ability levels
• Does not require • Sometimes requires • Usually requires learners to • Always requires learners
learners to become actively learners to become actively become actively engaged to become actively engaged
engaged engaged in order to learn
• Text and documents do • Text and documents • Text and documents • Text and documents
(g)
not employ multimedia sometimes employ usually employ multimedia always employ multimedia
enhancements to make multimedia enhancements to enhancements to make enhancements to make
learning interactive make learning interactive learning interactive learning interactive
• Does not provide • Provides minimal • Provides some feedback • Provides appropriate
feedback throughout the feedback throughout the throughout the instruction feedback throughout the
instruction instruction instruction
• Does not motivate the • Rarely motivates learner• Often motivates the learner • Keenly motivates the
learner to continue learning to continue learning and learner to continue learning
master concepts and master concepts
4. • Program provides little or • Program offers limited • Program offers various • Program offers help at
no help to the teacher or the options for help forms of help for the student any stage
student but may not be quickly
accessible
• Tech support is • Program offers online • Program often provides • Provides various ways to
inadequate or unreliable support only ways to reach tech support reach technical support
• Program does not offer • Student support • Program provides student • Program provides
support materials or outside materials are limited and do with additional websites which students with additional
(h)
means of reinforcement not relate directly to the relate to the lesson resources such as web
lesson sites, bibliographies, etc.
which are suitable to lesson
• Teachers and students • Teachers and students • Teachers and students can • Teachers and students
are not able to track can sometimes track a frequently track a student's can easily track a student's
progress student's progress through progress through feedback or progress through feedback
feedback or other other documentation or other documentation
documentation
• Assessment is • Assessment is • Assessment is usually • Assessment methods are
inappropriate or unavailable inappropriate or unrelated to challenging and appropriate challenging, appropriate,
and does not produce an learning goals and rarely enough to engage learners and suited to learning goals
accurate account of student engages learners
(i)
learning
• It is not clear how to • Teachers must develop • Teachers can assess • Teachers can easily
assess the learning in this their own assessments students' progress using assess students' progress
product established methods of by evaluating the outcomes
assessment provided within the product
• Reading level is not • Reading level is often • Reading level is appropriate• Reading level is
appropriate for target too difficult or too easy for for target audience, but some appropriate for target
audience target audience portions may be too easy or audience
too difficult
• Product is not suitable • Many features are • Most features are suitable • Product is suitable for the
(j)
for the age and grade level unsuitable for the age and for the age and grade level age and grade level
grade level
• Directions are • Directions are • Most directions are clear, • Directions are clear and
inadequate and incomplete sometimes unclear or but some are ambiguous or complete enough for
ambiguous confusing students to perform
required tasks
• Learners are unable to • Learners can save at • Learners can save at some • Learners can save at
save at regular intervals some point but can not re- point and can usually re-enter regular intervals and re-
(k)
enter the instruction without the instruction easily enter the instruction at any
difficulty point
5. • Cannot be integrated into • Some aspects of the • Most aspects of the • All aspects of the
classroom activities software can be integrated software can be integrated software can be easily
into classroom activities into classroom activities integrated into classroom
activities
• It is unclear how this • Few lessons can be • The program includes • The program features
program would be used with used in a variety of suggestions for use in whole activities for use in whole
students; contains no classroom settings; Includes class instruction, individual, or class instruction, individual,
guidelines or suggestions for few suggestions for altering group learning experiences or group learning
alternative classroom instruction for whole class, experiences
settings individual, or group
experiences
Total Points
Scale 40-45 = Exemplary 35-39 = Good 30-34 = Satisfactory <30 = Unacceptable