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.
IPQC checks are carried out during the manufacturing process to monitor critical variables that can impact product quality. In-process materials are tested for identity, strength, and purity, and any rejected materials are quarantined. The objectives are quality control, process control, and ensuring final product quality through continuous monitoring and implementation of good manufacturing practices. IPQC involves establishing and documenting controls to ensure output falls within acceptable standard ranges.
The narcotic drugs and psychotropic substances (NDPS) act, 1985 and rules, 1985Ravish Yadav
The document provides an overview of the Narcotic Drugs and Psychotropic Substances Act of 1985 in India. It defines key terms like cannabis, opium, and illicit trafficking. It describes the objectives of the act to control narcotics and implement international drug conventions. It outlines the various authorities and committees established under the act, such as the Narcotic Drugs and Psychotropic Substances Consultative Committee. It also summarizes the major provisions of the act regarding prohibitions, offenses and penalties for drug crimes.
Drugs and magic remedies act (objectionable advertisements) 1954Sanchita Mahale
This document summarizes the Drugs and Magic Remedies (Objectionable Advertisements) Act, 1954 of India. It discusses examples of misleading advertisements, objectives of the act, key definitions, classes of prohibited and exempted advertisements, offenses and penalties. Specifically, it prohibits advertisements for cures or treatments of certain diseases unless scientific evidence is provided, and bans advertisements for magic remedies. Exempted advertisements include those sent confidentially to medical practitioners or published in scientific literature. Contravention of the act may result in fines or imprisonment.
Plant layout of capsules contains the defination, types, layout of hard and soft gelatin capsule and the environmental condition concluding with the references.
This document outlines a change control system for Julphar Pharmaceuticals PLC in Ethiopia. It defines what constitutes a change, describes the change control process, and categorizes changes as minor, major, or critical. The change control process ensures changes are documented, evaluated, approved, implemented effectively and do not negatively impact safety, quality or regulatory compliance. Emergency changes require notification to quality assurance within 24 hours and products affected must be placed on hold until approved.
- The document provides a history of medical device regulation in the United States, European Union, and India.
- It outlines key milestones and developments in legislation and regulatory bodies governing medical devices in each region from the early 1900s to present day.
- Major acts and directives established regulatory frameworks and agencies to oversee safety and efficacy of medical devices, with increasing oversight and standards over time.
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.
IPQC checks are carried out during the manufacturing process to monitor critical variables that can impact product quality. In-process materials are tested for identity, strength, and purity, and any rejected materials are quarantined. The objectives are quality control, process control, and ensuring final product quality through continuous monitoring and implementation of good manufacturing practices. IPQC involves establishing and documenting controls to ensure output falls within acceptable standard ranges.
The narcotic drugs and psychotropic substances (NDPS) act, 1985 and rules, 1985Ravish Yadav
The document provides an overview of the Narcotic Drugs and Psychotropic Substances Act of 1985 in India. It defines key terms like cannabis, opium, and illicit trafficking. It describes the objectives of the act to control narcotics and implement international drug conventions. It outlines the various authorities and committees established under the act, such as the Narcotic Drugs and Psychotropic Substances Consultative Committee. It also summarizes the major provisions of the act regarding prohibitions, offenses and penalties for drug crimes.
Drugs and magic remedies act (objectionable advertisements) 1954Sanchita Mahale
This document summarizes the Drugs and Magic Remedies (Objectionable Advertisements) Act, 1954 of India. It discusses examples of misleading advertisements, objectives of the act, key definitions, classes of prohibited and exempted advertisements, offenses and penalties. Specifically, it prohibits advertisements for cures or treatments of certain diseases unless scientific evidence is provided, and bans advertisements for magic remedies. Exempted advertisements include those sent confidentially to medical practitioners or published in scientific literature. Contravention of the act may result in fines or imprisonment.
Plant layout of capsules contains the defination, types, layout of hard and soft gelatin capsule and the environmental condition concluding with the references.
This document outlines a change control system for Julphar Pharmaceuticals PLC in Ethiopia. It defines what constitutes a change, describes the change control process, and categorizes changes as minor, major, or critical. The change control process ensures changes are documented, evaluated, approved, implemented effectively and do not negatively impact safety, quality or regulatory compliance. Emergency changes require notification to quality assurance within 24 hours and products affected must be placed on hold until approved.
- The document provides a history of medical device regulation in the United States, European Union, and India.
- It outlines key milestones and developments in legislation and regulatory bodies governing medical devices in each region from the early 1900s to present day.
- Major acts and directives established regulatory frameworks and agencies to oversee safety and efficacy of medical devices, with increasing oversight and standards over time.
The document summarizes recent advancements in Indian drug regulations regarding amendments to Schedule M. It provides an overview of the Central Drugs Standard Control Organization (CDSCO) and its geographical locations across India. It then discusses the background and content of the existing Schedule M-2001 and the proposed Draft Schedule M-2018, highlighting new additions around pharmaceutical quality systems, quality risk management, and change control. Key features of the draft include expanded requirements for suppliers, stability studies, and continual improvement in quality systems.
The European Medicines Agency (EMA) regulates medicines for human and veterinary use in Europe. Based in London, the EMA ensures medicines are safe and effective, working with authorities in EU member states. Over its 25 year history, the EMA has authorized over 1000 human and 200 veterinary medicines. While facilitating timely access to medicines, the EMA monitors safety and provides information to healthcare professionals and patients, but does not regulate pricing, advertising, patents, or certain other products. The EMA comprises several scientific committees and is supported by the European Directorate for Quality of Medicines.
This document discusses drug master files (DMFs), which contain confidential information submitted to the FDA about a drug's chemistry, manufacturing, and controls. There are 5 types of DMFs:
Type I contains information about a manufacturing site and facilities. Type II contains details about drug substances and intermediates. Type III covers packaging materials. Type IV is for excipients and materials used in their preparation. Type V is for reference information not covered in the other types, like clinical or toxicity data, after discussion with the FDA. A DMF is submitted voluntarily to support applications like an IND, NDA, or ANDA, but is not itself approved or disapproved. It provides confidential information that can be referenced in
The document summarizes key aspects of the Drug and Cosmetic Act and Rules in India, including:
- The Acts and Rules regulate the import, manufacture, distribution and sale of drugs and cosmetics in India.
- Important definitions are provided for terms like "drug", "cosmetic", "manufacture" and others.
- Drugs and cosmetics can be deemed "misbranded", "adulterated" or "spurious" if they do not meet certain standards.
- The Rules contain 18 parts and 26 schedules providing detailed requirements and guidelines for drugs and cosmetics.
- Key agencies like the Drugs Technical Advisory Board help administer the Acts and
The document summarizes ICH Q8 guidelines for pharmaceutical product development using a Quality by Design (QbD) approach. It discusses key QbD concepts like quality target product profiles, critical quality attributes, critical process parameters, and design space. The guidelines suggest determining aspects of drug substances, excipients, manufacturing processes, and container closure systems that are critical to quality. They provide guidance on contents for drug product development documentation, including formulation development, compatibility studies, container closure selection, and ensuring microbiological attributes and stability. The QbD approach aims to build quality into pharmaceutical products from the design stage through understanding and control of material and process variables.
A primary mission of the Food and Drug Administration is to conduct comprehensive regulatory coverage of all aspects of production and distribution of drugs and drug products to assure that such products meet the 501(a)(2)(B) requirements of the Act. FDA has developed two basic strategies:
. 1) evaluating through factory inspections, including the collection and analysis of associated samples, the conditions and practices under which drugs and drug products are manufactured, packed, tested and held, and
. 2) monitoring the quality of drugs and drug products through surveillance activities such as sampling and analyzing products in distribution.
FDA compliance program “ Drug Manufacturing Inpsections” (7356.002) is designed to provide guidance for implementing the first strategy. Products from production and distribution facilities covered under this program are consistently of acceptable quality if the firm is operating in a state of control.
The inspectional guidance in this program is structured to provide for efficient use of resources devoted to routine surveillance coverage, recognizing that in-depth coverage of all systems and all processes is not feasible for all firms on a biennial basis. It also provides for follow-up compliance coverage as needed.
“Drug Regulations” has prepared a summary from the compliance programme and is given below in the presentation.
Drug labeling in India is regulated by the Drugs and Cosmetics Rules 1945. All drug labels must conform to these specifications and include information like the drug name, quantity, active ingredients, manufacturer details, batch number, expiration date and storage conditions. Prescription drug labels have additional requirements depending on the drug schedule. Package inserts provide directions for safe use to healthcare professionals. Proper drug labeling is important for the safe use of medicines.
This document discusses the responsibilities of Marketing Authorization Holders (MAHs) in Japan. It explains that MAHs must have a suitable quality control system called Good Quality Practice (GQP) and a suitable safety control system after manufacturing called Good Vigilance Practice (GVP). The GQP ensures quality assurance of medical devices, while the GVP standardizes the practice for safety control, such as collecting and evaluating safety information. The document also provides an overview of the GQP organization structure and reporting requirements under GVP.
The document summarizes the Drugs and Cosmetics Act of 1940 and Rules of 1945 in India. Some key points:
- It was enacted to regulate the import, manufacture, distribution and sale of drugs and cosmetics through a licensing system. Only qualified persons can manufacture, distribute and sell drugs and cosmetics.
- It covers definitions of drugs and cosmetics. Provisions relate to import, manufacture, sale, labeling and packaging of drugs. It describes schedules to the act and amendments made over time.
- The act is administered through various advisory committees and authorities like the Drugs Technical Advisory Board and Drugs Control Laboratories. It outlines licensing, manufacturing and sale requirements for different drug categories
The document defines a master formula record as specifying starting materials, quantities, packaging materials, and processing instructions to produce a finished product batch. It outlines the requirements for a master formula record including: (1) product name and reference code, composition, strength, and batch size; (2) processing location and equipment; (3) starting materials and quantities; (4) expected final yield and intermediate yields; and (5) detailed processing, storage, and packaging instructions. International guidelines from WHO, EU, PIC, Canada, and USA provide further requirements for master formula record contents.
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.
THE DRUGS AND COSMETICS ACT 1940 AND RULES 1945Milan Dajjuka
The document summarizes the Drugs and Cosmetics Act of 1940 and Rules of 1945 in India. It outlines the history and objectives of regulating drugs and cosmetics through licensing. It defines key terms like drugs, cosmetics, misbranded drugs, adulterated drugs, and spurious drugs. It also describes the administration of the act through bodies like the Drugs Technical Advisory Board, Drugs Consultative Committee, and Central Drugs Laboratory. The act aims to ensure quality standards for drugs and cosmetics in India.
Drug and magic remedies (objectionable advertisement) act 1954 and rules 1955Dr. Ambekar Abdul Wahid
Definitions, Class of Prohibitions Advertisement - Section 3, Classes of exempted advertisements, Powers of entry, search etc., Offenses and penalties, Scrutiny of misleading advertisements relating to drugs, Manner in which advertisements may be sent confidentially, Case Studies.
The document provides guidelines for regulating herbal medicines in Europe and Japan. In Europe, herbal medicinal products are regulated and must comply with guidelines on quality control, safety, efficacy, advertising and more. Herbal medicines from foreign countries entering the market must also provide proof of quality, safety and efficacy. In Japan, traditional herbal medicines called Kampo are regulated similarly to conventional drugs, and must undergo clinical trials and comply with good manufacturing practices. Japan also has various systems for monitoring adverse reactions to herbal medicines. The regulatory frameworks aim to standardize quality while allowing traditional herbal approaches to be practiced legally.
Introduction to D & C Act 1940 and Rules 1945, Definitions, Various Schedules in D & C Rules 1945, Administration of the act and rules, Manufacturing , Distribution and sale of drug and cosmetic, Labeling and Packing of drug and cosmetic.
Change control is a formal system to review proposed and actual changes that could affect a product's validated status. It aims to determine if actions are needed to maintain validation. Changes are classified as minor, major, or critical based on their potential safety/efficacy impact. Approval levels 1-3 require sign-off from different departments. The change control procedure involves documenting changes using a form, assessing the need and approving/rejecting changes, planning implementation, verifying the implementation, and closing the change request once complete.
Pharmacovigilance is the science of monitoring the effects of pharmaceutical products after they have been licensed for use, especially in order to identify and evaluate previously unreported adverse reactions. Herb-drug interactions can occur when herbs are taken concurrently with prescription or over-the-counter medications. Some common herb-drug interactions include garlic increasing the breakdown of antiviral drugs, green tea increasing the side effects of oral contraceptives, and liquorice decreasing the effectiveness of antihypertensives. It is important to report any suspected adverse reactions to medications to help ensure safe and effective use of drugs and herbs.
Second Party Audit and External Third Party AuditShantanuThakre3
Second Party Audit:- Second-party audit is when a company performs an audit of a supplier to ensure that they are meeting the requirements specified in the contract.
External Third Party Audit:-
A third-party audit occurs when a company has decided that they want to create a Quality Management System (QMS) that conforms to a standard set of requirements, such as ISO 9001 and hire an independent auditing company to perform an audit to verify that the company has succeeded in meeting these standards.
The Medical Device Single Audit Program (MDSAP) is an initiative by the International Medical Device Regulators Forum (IMDRF) to develop a harmonized audit program that allows medical device manufacturers to undergo a single regulatory audit to satisfy the requirements of multiple regulatory jurisdictions. The MDSAP pilot program began in 2014 and involves regulators from the US, Canada, Brazil, Australia and Japan. It aims to recognize third-party auditing organizations to conduct audits of medical device manufacturers according to a standardized audit process, with the goal of facilitating medical device trade while ensuring public health and safety.
This document defines key terms related to Good Manufacturing Practice (GMP) for pharmaceuticals. It discusses GMP requirements for facilities, equipment, documentation, materials, processes, quality control, quality assurance, personnel, sanitation, complaints, and recalls. Key points include that GMP aims to consistently produce quality medicines through validated processes and facilities, qualified staff, appropriate materials and equipment, and defined procedures. Quality assurance covers all activities influencing quality, while quality control tests and releases products. Personnel must be properly trained and hygienic practices followed.
The document summarizes recent advancements in Indian drug regulations regarding amendments to Schedule M. It provides an overview of the Central Drugs Standard Control Organization (CDSCO) and its geographical locations across India. It then discusses the background and content of the existing Schedule M-2001 and the proposed Draft Schedule M-2018, highlighting new additions around pharmaceutical quality systems, quality risk management, and change control. Key features of the draft include expanded requirements for suppliers, stability studies, and continual improvement in quality systems.
The European Medicines Agency (EMA) regulates medicines for human and veterinary use in Europe. Based in London, the EMA ensures medicines are safe and effective, working with authorities in EU member states. Over its 25 year history, the EMA has authorized over 1000 human and 200 veterinary medicines. While facilitating timely access to medicines, the EMA monitors safety and provides information to healthcare professionals and patients, but does not regulate pricing, advertising, patents, or certain other products. The EMA comprises several scientific committees and is supported by the European Directorate for Quality of Medicines.
This document discusses drug master files (DMFs), which contain confidential information submitted to the FDA about a drug's chemistry, manufacturing, and controls. There are 5 types of DMFs:
Type I contains information about a manufacturing site and facilities. Type II contains details about drug substances and intermediates. Type III covers packaging materials. Type IV is for excipients and materials used in their preparation. Type V is for reference information not covered in the other types, like clinical or toxicity data, after discussion with the FDA. A DMF is submitted voluntarily to support applications like an IND, NDA, or ANDA, but is not itself approved or disapproved. It provides confidential information that can be referenced in
The document summarizes key aspects of the Drug and Cosmetic Act and Rules in India, including:
- The Acts and Rules regulate the import, manufacture, distribution and sale of drugs and cosmetics in India.
- Important definitions are provided for terms like "drug", "cosmetic", "manufacture" and others.
- Drugs and cosmetics can be deemed "misbranded", "adulterated" or "spurious" if they do not meet certain standards.
- The Rules contain 18 parts and 26 schedules providing detailed requirements and guidelines for drugs and cosmetics.
- Key agencies like the Drugs Technical Advisory Board help administer the Acts and
The document summarizes ICH Q8 guidelines for pharmaceutical product development using a Quality by Design (QbD) approach. It discusses key QbD concepts like quality target product profiles, critical quality attributes, critical process parameters, and design space. The guidelines suggest determining aspects of drug substances, excipients, manufacturing processes, and container closure systems that are critical to quality. They provide guidance on contents for drug product development documentation, including formulation development, compatibility studies, container closure selection, and ensuring microbiological attributes and stability. The QbD approach aims to build quality into pharmaceutical products from the design stage through understanding and control of material and process variables.
A primary mission of the Food and Drug Administration is to conduct comprehensive regulatory coverage of all aspects of production and distribution of drugs and drug products to assure that such products meet the 501(a)(2)(B) requirements of the Act. FDA has developed two basic strategies:
. 1) evaluating through factory inspections, including the collection and analysis of associated samples, the conditions and practices under which drugs and drug products are manufactured, packed, tested and held, and
. 2) monitoring the quality of drugs and drug products through surveillance activities such as sampling and analyzing products in distribution.
FDA compliance program “ Drug Manufacturing Inpsections” (7356.002) is designed to provide guidance for implementing the first strategy. Products from production and distribution facilities covered under this program are consistently of acceptable quality if the firm is operating in a state of control.
The inspectional guidance in this program is structured to provide for efficient use of resources devoted to routine surveillance coverage, recognizing that in-depth coverage of all systems and all processes is not feasible for all firms on a biennial basis. It also provides for follow-up compliance coverage as needed.
“Drug Regulations” has prepared a summary from the compliance programme and is given below in the presentation.
Drug labeling in India is regulated by the Drugs and Cosmetics Rules 1945. All drug labels must conform to these specifications and include information like the drug name, quantity, active ingredients, manufacturer details, batch number, expiration date and storage conditions. Prescription drug labels have additional requirements depending on the drug schedule. Package inserts provide directions for safe use to healthcare professionals. Proper drug labeling is important for the safe use of medicines.
This document discusses the responsibilities of Marketing Authorization Holders (MAHs) in Japan. It explains that MAHs must have a suitable quality control system called Good Quality Practice (GQP) and a suitable safety control system after manufacturing called Good Vigilance Practice (GVP). The GQP ensures quality assurance of medical devices, while the GVP standardizes the practice for safety control, such as collecting and evaluating safety information. The document also provides an overview of the GQP organization structure and reporting requirements under GVP.
The document summarizes the Drugs and Cosmetics Act of 1940 and Rules of 1945 in India. Some key points:
- It was enacted to regulate the import, manufacture, distribution and sale of drugs and cosmetics through a licensing system. Only qualified persons can manufacture, distribute and sell drugs and cosmetics.
- It covers definitions of drugs and cosmetics. Provisions relate to import, manufacture, sale, labeling and packaging of drugs. It describes schedules to the act and amendments made over time.
- The act is administered through various advisory committees and authorities like the Drugs Technical Advisory Board and Drugs Control Laboratories. It outlines licensing, manufacturing and sale requirements for different drug categories
The document defines a master formula record as specifying starting materials, quantities, packaging materials, and processing instructions to produce a finished product batch. It outlines the requirements for a master formula record including: (1) product name and reference code, composition, strength, and batch size; (2) processing location and equipment; (3) starting materials and quantities; (4) expected final yield and intermediate yields; and (5) detailed processing, storage, and packaging instructions. International guidelines from WHO, EU, PIC, Canada, and USA provide further requirements for master formula record contents.
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.
THE DRUGS AND COSMETICS ACT 1940 AND RULES 1945Milan Dajjuka
The document summarizes the Drugs and Cosmetics Act of 1940 and Rules of 1945 in India. It outlines the history and objectives of regulating drugs and cosmetics through licensing. It defines key terms like drugs, cosmetics, misbranded drugs, adulterated drugs, and spurious drugs. It also describes the administration of the act through bodies like the Drugs Technical Advisory Board, Drugs Consultative Committee, and Central Drugs Laboratory. The act aims to ensure quality standards for drugs and cosmetics in India.
Drug and magic remedies (objectionable advertisement) act 1954 and rules 1955Dr. Ambekar Abdul Wahid
Definitions, Class of Prohibitions Advertisement - Section 3, Classes of exempted advertisements, Powers of entry, search etc., Offenses and penalties, Scrutiny of misleading advertisements relating to drugs, Manner in which advertisements may be sent confidentially, Case Studies.
The document provides guidelines for regulating herbal medicines in Europe and Japan. In Europe, herbal medicinal products are regulated and must comply with guidelines on quality control, safety, efficacy, advertising and more. Herbal medicines from foreign countries entering the market must also provide proof of quality, safety and efficacy. In Japan, traditional herbal medicines called Kampo are regulated similarly to conventional drugs, and must undergo clinical trials and comply with good manufacturing practices. Japan also has various systems for monitoring adverse reactions to herbal medicines. The regulatory frameworks aim to standardize quality while allowing traditional herbal approaches to be practiced legally.
Introduction to D & C Act 1940 and Rules 1945, Definitions, Various Schedules in D & C Rules 1945, Administration of the act and rules, Manufacturing , Distribution and sale of drug and cosmetic, Labeling and Packing of drug and cosmetic.
Change control is a formal system to review proposed and actual changes that could affect a product's validated status. It aims to determine if actions are needed to maintain validation. Changes are classified as minor, major, or critical based on their potential safety/efficacy impact. Approval levels 1-3 require sign-off from different departments. The change control procedure involves documenting changes using a form, assessing the need and approving/rejecting changes, planning implementation, verifying the implementation, and closing the change request once complete.
Pharmacovigilance is the science of monitoring the effects of pharmaceutical products after they have been licensed for use, especially in order to identify and evaluate previously unreported adverse reactions. Herb-drug interactions can occur when herbs are taken concurrently with prescription or over-the-counter medications. Some common herb-drug interactions include garlic increasing the breakdown of antiviral drugs, green tea increasing the side effects of oral contraceptives, and liquorice decreasing the effectiveness of antihypertensives. It is important to report any suspected adverse reactions to medications to help ensure safe and effective use of drugs and herbs.
Second Party Audit and External Third Party AuditShantanuThakre3
Second Party Audit:- Second-party audit is when a company performs an audit of a supplier to ensure that they are meeting the requirements specified in the contract.
External Third Party Audit:-
A third-party audit occurs when a company has decided that they want to create a Quality Management System (QMS) that conforms to a standard set of requirements, such as ISO 9001 and hire an independent auditing company to perform an audit to verify that the company has succeeded in meeting these standards.
The Medical Device Single Audit Program (MDSAP) is an initiative by the International Medical Device Regulators Forum (IMDRF) to develop a harmonized audit program that allows medical device manufacturers to undergo a single regulatory audit to satisfy the requirements of multiple regulatory jurisdictions. The MDSAP pilot program began in 2014 and involves regulators from the US, Canada, Brazil, Australia and Japan. It aims to recognize third-party auditing organizations to conduct audits of medical device manufacturers according to a standardized audit process, with the goal of facilitating medical device trade while ensuring public health and safety.
This document defines key terms related to Good Manufacturing Practice (GMP) for pharmaceuticals. It discusses GMP requirements for facilities, equipment, documentation, materials, processes, quality control, quality assurance, personnel, sanitation, complaints, and recalls. Key points include that GMP aims to consistently produce quality medicines through validated processes and facilities, qualified staff, appropriate materials and equipment, and defined procedures. Quality assurance covers all activities influencing quality, while quality control tests and releases products. Personnel must be properly trained and hygienic practices followed.
Pharo 4 was released in Spring 2015, containing many improvements and updates since Pharo 3 in April 2014. These include improved refactorings, a dark theme, GT tools replacing old tools, first class variables, advanced reflection capabilities, Epicea replacing .changes, and a new GC called Spur. Future plans include a 64-bit COG VM, an optimizer called Sista, updated windowing with SDL2, a Block redo in Morphic, 3D with Woden, and a virtual GPU. Pharo remains very active with ongoing development and a welcoming community.
This document summarizes a talk on reflection in Pharo. It discusses how:
1) Everything can be represented as an object in Pharo, including code, through the use of abstract syntax trees (ASTs).
2) The AST is now deeply integrated in Pharo and easily accessible. Methods can be annotated by linking meta objects to nodes in the AST.
3) When the code is executed, the links are followed to modify the behavior, allowing aspects like breakpoints or coverage to be implemented through annotation of the AST.
Pharo is a Smalltalk dialect programming language. From the pharo-project.org website:
"Pharo's goal is to deliver a clean, innovative, open-source Smalltalk environment. By providing a stable and small core system, excellent developer tools, and maintained releases, Pharo is an attractive platform to build and deploy mission critical Smalltalk applications. Pharo is MIT licensed and is steered by a board of benevolent dictators. The board makes final decisions if no consensus can be reached within the community. Pharo fosters a healthy ecosystem of both private and commercial contributors who advance and maintain the core system and its external packages."
Smalltalk allows everything to be accessible and modifiable through a live programming environment. The system's objects can be understood and fixed directly. This contrasts with traditional languages where the programmer must mentally switch between documentation, libraries, and code. Smalltalk also provides a permissive license and community support through mailing lists and projects. While it takes adjustment to its different approach, Smalltalk aims to keep programming intuitive through its interactive, self-documenting nature.
Pharo is an open-source programming environment and language based on Smalltalk. It allows users to explore and change running systems through reflection. The language is object-oriented, dynamic, and reflective. Pharo started in 2008 as a fork of Squeak Smalltalk and has since had yearly releases. The environment provides tools like the class browser and inspector to manipulate classes, methods, and other objects that make up the system.
This document provides an overview of object-oriented programming concepts and the Smalltalk programming language. It discusses the essence of class-based object orientation, including classes, objects, encapsulation, inheritance and polymorphism. It then introduces the Smalltalk language, covering its history and development, core concepts like everything is an object and message passing, and how to get started programming in Smalltalk. Standard development tools and syntax like methods, statements, control structures and creating classes are also summarized.
Pharo is an immersive programming environment that aims to combat software complexity through an approach of running safe-to-fail experiments with fast feedback, adaptable tools, visibility of system state, and late binding that avoids early commitments. Pharo commits code late at runtime, allows objects to decide how to handle messages, supports test-driven "debugger driven" development, and is a small and simple environment where everything is an object that communicates through message passing. Pharo also emphasizes reuse through domain-specific languages, refactoring tools, and metaprogramming to rewrite code. It is an open source research vehicle and platform for commercial software.
This document provides an overview of the syntax and core concepts in Pharo. It discusses that Pharo has no constructors, types, interfaces, packages, or parametrized types. The core abstractions are objects like strings, numbers, collections, and blocks. Messages can be unary, binary, or take keywords. Control flow uses conditionals that send messages to booleans. Common loops include timesRepeat:, to:do:, and collect:. Defining methods involves subclassing and specifying instance/class variables.
Pharo is an open-source live programming environment and programming language started in 2008. The official web site is http://www.pharo-project.org. By providing a stable and small core system, excellent dev tools, and maintained releases, Pharo is an attractive platform to build and deploy mission-critical applications.
The Pharo Roadmap document outlines the community's ongoing and planned work to improve and develop the Pharo programming environment and ecosystem. Key areas of focus include improving the code model infrastructure, graphics library, compiler, serialization, scripting support, distributions, browser, and virtual machine. It also discusses plans for a Pharo consortium to help sustain the community's efforts through paid support.
Pharo uses a pure object-oriented model where everything is an object, including classes. There is single inheritance and only message passing between objects. Classes are objects themselves that are instances of metaclass objects. Method lookup involves searching the receiver's class and its superclass. Packages can contain methods defined on classes in other packages, providing flexibility.
This document compares the parallel programming support in Haskell, F#, and Scala by looking at their language features, high-level abstractions for parallelism, and experimental results from implementing the n-body problem on multi-core systems. It finds that all three languages provide good support for parallelism through features like parallel collections, tasks, actors, and strategies/skeletons. Haskell uses the par and pseq primitives as well as evaluation strategies. F# utilizes tasks from the Task Parallel Library and async workflows. Scala supports parallel collections and actors. Experimental results on implementing the n-body problem in the languages show they can all effectively utilize multiple cores.
The document discusses the singleton design pattern, which ensures a class only has one instance and provides a global access point to it. It describes the problem of wanting a class with a single instance and the solution of storing the first instance created and returning it each time. Examples are provided using a DBConnect class. Implementation details covered include using a class variable to store the instance, ensuring only one instance can be created, and whether to use a class variable or instance variable to store the singleton. The document also discusses issues like whether to favor instance behavior over class behavior for singletons.
Oracle provides a comprehensive cloud infrastructure platform with compute, storage, networking and database services. Key features include fast NVMe SSD storage both locally and network attached, high performance bare metal and VM instances with GPU and AMD EPYC options, autonomous database services, and advanced networking capabilities like low latency and RDMA. Oracle's regional architecture and dedicated fast interconnects enable high availability across availability domains and regions.
This document provides a high-level overview of a cloud architecture design. It discusses considerations for the design including service assurance, high availability, secure tenant segregation, and data center scalability. It then describes the proposed design which includes pods, availability zones, and regions to provide modular scalability, redundancy, and tenant isolation. Management servers and databases are separated for control and data planes.
The Kubernetes WebLogic revival (part 1)Simon Haslam
This document provides an overview of WebLogic 12c and discusses its deployment in cloud environments. It begins with introductions to Java Enterprise Edition, WebLogic server, and WebLogic clustering. It then covers virtualization technologies like containers and Docker. The document discusses various options for provisioning WebLogic in the cloud, including using Java Cloud Service, the Oracle Cloud Infrastructure marketplace, and Kubernetes. It concludes by looking at future directions for WebLogic and Kubernetes integration.
Data Engineer, Patterns & Architecture The future: Deep-dive into Microservic...Igor De Souza
With Industry 4.0, several technologies are used to have data analysis in real-time, maintaining, organizing, and building this on the other hand is a complex and complicated job. Over the past 30 years, we saw several ideas to centralize the database in a single place as the united and true source of data has been implemented in companies, such as Data wareHouse, NoSQL, Data Lake, Lambda & Kappa Architecture.
On the other hand, Software Engineering has been applying ideas to separate applications to facilitate and improve application performance, such as microservices.
The idea is to use the MicroService patterns on the date and divide the model into several smaller ones. And a good way to split it up is to use the model using the DDD principles. And that's how I try to explain and define DataMesh & Data Fabric.
Automated Deployment and Management of Edge CloudsJay Bryant
This presentation discusses the challenges of cloud computing at the edge. From the exploding number of nodes, the need for integrated monitoring and zero touch discovery. We introduce Lenovo Open Cloud Automation, an automated framework built in collaboration with Red Hat to help address these challenges.
The document summarizes Oracle's SuperCluster engineered system. It provides consolidated application and database deployment with in-memory performance. Key features include Exadata intelligent storage, Oracle M6 and T5 servers, a high-speed InfiniBand network, and Oracle VM virtualization. The SuperCluster enables database as a service with automated provisioning and security for multi-tenant deployment across industries.
This document is a curriculum vitae for Senthilnadhan K that summarizes his professional experience and qualifications. He has over 7 years of experience in storage management, including administration of EMC, Hitachi, and SUN storage systems. Currently he works as an IT analyst for Tata Consultancy Services where he is responsible for storage administration, replication, migration, and troubleshooting. Previously he worked as a senior system administrator for HCL Infosystems where he managed SUN and IBM storage arrays and SAN fabrics.
Containers and microservices create new performance challenges kowall - app...Jonah Kowall
AppSphere 2015 presentation on the challenges brought forth by Microservices and Containers such as Docker. Goes into OSS and commercial tools to manage availability and performance.
AppSphere 15 - Containers and Microservices Create New Performance ChallengesAppDynamics
Jonah Kowall, VP of Market Development and Insights, outlines what needs to be built in terms of data extraction, analytics, and other open source technologies. Finally we’ll also discuss commercial alternatives and what features and functions are critical when monitoring microservices based applications. This presentation is from AppSphere 2015.
This presentation shares a clear understanding of:
- What is changing with software, and why?
- What challenges are faced with these changes?
- How to overcome these challenges
DockerCon EU 2015: Using Docker and SDN for telco-grade applicationsDocker, Inc.
Presented by Nico Janssens, Senior Researcher, Bell Labs, Alcatel-Lucent and Florian Otel, Director for Business Development and Strategy, Nuage Networks
In this talk we will present how at Bell-Labs (Alcatel-Lucent R&D division) we benefit from using Docker in combination with the SDN solution from Nuage Networks for development and deployment of a next-gen chat-based communication platform. This communication platform does intensive data analytics, runs a number of multi-media services and can control remote appliances (e.g. thermostats, robots, cameras, etc). We will illustrate the stringent telco requirements to successfully operate such a communication platform, including some non-functional needs like high-availability, reliability, elasticity, QoS and lifecycle management. Furthermore, we will explain why we selected docker as a hosting platform and how we have utilized it. We will also share some of the deployment scenarios we are facing and how these are addressed by combining Docker and Nuage VSP. Lastly, we will share the lessons we have learned during this development process, and propose some improvements/extensions for Docker to evolve into an application stack that is able to meet the stringent needs of telco applications.
Stay productive while slicing up the monolithMarkus Eisele
The document discusses strategies for evolving monolithic applications into microservice architectures. It notes that modern software needs to meet increasing demands around release frequency, developer velocity, and infrastructure costs. While classical architectures based on monoliths and service-oriented architectures were effective, they no longer address today's challenges. The document then introduces microservices as an alternative, describing characteristics like independent deployability, language/data agnosticism, and process isolation. It acknowledges that while building individual microservices is straightforward, the difficult part is designing the overall system architecture and operational capabilities required to manage many interconnected microservices. Lagom is presented as one framework that can help implement reactive microservices on the JVM.
Shahnawaz Ali has over 12 years of experience managing IT infrastructure projects internationally. His career summary highlights experience with strategic performance management including datacenter planning, virtualization, cloud computing, storage solutions, networking and security. He has worked extensively on projects related to development, evaluation, datacenter planning and management, server/network/security planning, and disaster recovery. His technical responsibilities have included building solutions for tiered datacenters, cloud migration, virtualization, storage, networking, security and more.
Stay productive while slicing up the monolithMarkus Eisele
Microservices-based architectures are in vogue. Over the last couple of years, we have learned how thought leaders implement them, and it seems like every other week we hear about how containers and platform-as-a-service offerings make them ultimately happen.
Tech Talent Night Copenhagen 11/22/17
https://greenticket.dk/techtalentnightcph
ITCamp 2011 - Mihai Nadas - Windows Azure interopITCamp
The document discusses running various technologies like Java, PHP, and MySQL on the Windows Azure platform. It begins with an overview of Windows Azure and how it allows users to run full operating system virtual machines in the cloud. It then demonstrates running Java applications like Tomcat on Windows Azure either using a preconfigured solution accelerator or manually configuring it within a worker role. Similarly, it shows how to run PHP applications by supplying the PHP runtime within a web role. It also discusses running MySQL in a worker role and provides solutions for configuring replication and high availability. The document advocates that Windows Azure allows developers freedom of choice in technologies by enabling many common languages and databases to run on its infrastructure.
20191201 kubernetes managed weblogic revival - part 1makker_nl
This document provides an overview of WebLogic 12c and discusses its deployment in cloud environments. It begins with an introduction to WebLogic and its core components like the administration server and clustering. It then covers virtualization technologies like containers and Docker, comparing them with traditional virtualization. Finally, it discusses different approaches for deploying WebLogic in the cloud like Java Cloud Service, Oracle Cloud Marketplace images, and Kubernetes; and looks at future directions like the WebLogic Kubernetes operator.
Rajnish Tyagi has over 11 years of experience in storage administration and management. He has expertise in IBM, EMC, NetApp, and HP storage solutions including DS8000, SVC, V7000, VNX, XtremIO, RecoverPoint, StoreVirtual, EVA, and 3PAR. He is skilled in storage configuration, provisioning, replication, troubleshooting, and scripting using Perl, PHP, Linux shell, and PowerShell. Currently he works as a consultant for HCL where he is responsible for storage implementations, DR setups, fabric migrations, and addressing storage-related issues for European clients.
Achhar Kalia has nearly 5 years of experience in application development, production support, and system integration. He has expertise in Linux/Unix administration, virtualization, databases, and networking. Some of his key skills include OpenStack, Oracle, DB2, networking protocols, and Ericsson products. He has worked on projects for clients such as Ericsson, Tata Consultancy Services, and Telstra involving the development, support and enhancement of various applications.
Idera live 2021: Managing Databases in the Cloud - the First Step, a Succes...IDERA Software
You need to start moving some on-premises databases to the cloud.
- Where do you begin?
- What are your options?
- What will your job look like afterward?
-What tools can you use to manage databases in the cloud?
- How does troubleshooting database performance problems in the cloud differ from on-premise?
- How can you help manage monthly cloud costs so the effort actually is cost effective?
Moving to the cloud is not as easy as one might think. So, knowing the answers to these kinds of question will place your feet on the path to success. See how DB PowerStudio can readily assist with these efforts and questions.
The presenter, Bert Scalzo, is an Oracle ACE, blogger, author, speaker and database technology consultant. He has worked with all major relational databases, including Oracle, SQL Server, Db2, Sybase, MySQL, and PostgreSQL. Bert’s work experience includes stints as product manager for multiple-database tools, such as DBArtisan and Aqua Data Studio at IDERA. He has three decades of Oracle database experience and previously worked for both Oracle Education and Oracle Consulting. Bert holds several Oracle Masters certifications and his academic credentials include a BS, MS, and PhD in computer science, as well as an MBA.
Workshop: Identifying concept inventories in agile programmingESUG
This document discusses the development of a concept inventory to identify common misconceptions in agile programming and object-oriented development. The project aims to strengthen collaboration between INRIA/Lille and ÉTS/UQAM by creating a concept inventory that can be used to improve teaching of agile development with object-oriented languages like TypeScript, JavaScript, and Pharo. The methodology involves identifying misconceptions, proposing a concept inventory, and validating it in courses by measuring understanding before and after instruction. A workshop will help identify initial misconceptions in Smalltalk/Pharo by capturing them in a collaborative tool.
This document proposes integrating documentation into the Pharo language metamodel and environment to improve documentation support. It suggests making documentation first-class citizens in Pharo by providing built-in support and a minimal API, which would allow tight integration with development tools and future extensions without requiring grammar changes or large efforts. This could improve documentation quality by enabling direct references between code and documentation and automatic logging of documentation usage.
The Pharo Debugger and Debugging tools: Advances and RoadmapESUG
This document outlines advances and the roadmap for debugging tools in Pharo. It discusses recent improvements to the debugging infrastructure, including architectural changes and new debugging commands. It also describes upcoming work, such as additional infrastructure improvements, an emergency debugger, support for meta-object protocols, a redesigned user experience, a remote debugger, and improved documentation. The document concludes by inviting participants to help evaluate new debugging experiments.
The document describes Sequence, a pipeline modeling and discrete event simulation framework developed in Pharo Smalltalk. Sequence allows describing system resources, building blocks that use those resources, assembling scenarios from blocks, collecting information during simulated runs, and interactively exploring system traces. The framework implements a discrete event simulation engine with event streams that model periodic processes and resources. Sequence provides tools for evaluating system performance through simulation before complete hardware is available.
Migration process from monolithic to micro frontend architecture in mobile ap...ESUG
This document discusses migrating a monolithic mobile application called CARL Touch to a micro frontend architecture. It presents a migration process involving three steps: 1) analysis of the monolithic codebase, 2) identification of potential micro frontends, and 3) transformation of the codebase to implement the identified micro frontends. Previous experiments at Berger-Levrault involving two teams migrating CARL Touch provided insights. The proposed process uses static and dynamic analysis, code visualization and clustering techniques to help identify optimal micro frontends and transform the codebase in a semi-automated manner.
Analyzing Dart Language with Pharo: Report and early resultsESUG
This document summarizes an analysis of the Dart programming language using tools in the Pharo environment. It describes generating a parser for Dart using SmaCC, which produces an AST. It also details defining a Famix meta-model for Dart and the Chartreuse-D importer that creates a FamixDart model from the AST. Future work is outlined, including improving SmaCCDart, continuing to develop the FamixDart meta-model, and handling dynamic types when importing associations. The goal is to analyze Dart and explore modeling Flutter applications.
Transpiling Pharo Classes to JS ECMAScript 5 versus ECMAScript 6ESUG
This document summarizes research on transpiling Pharo classes to JavaScript using ECMAScript 5 versus ECMAScript 6. It finds that transpiling to ES6 provides benefits like significantly faster load times, improved benchmark performance up to 43%, and more idiomatic code compared to ES5. However, fully emulating Smalltalk semantics like metaclass inheritance remains challenging when targeting JavaScript.
The document presents an approach for automated test generation from software models and execution traces. Key aspects of the approach include using metamodels to represent the codebase, values, and desired unit test structure. Models are built from the codebase and traces, then transformations are applied to generate unit tests conforming to the test metamodel. Abstract syntax trees are used to export the generated tests to code. The approach aims to generate tests that are relevant, readable and maintainable without relying on existing tests. An example demonstrates generating a JUnit test from an application class.
Genetic programming is used to generate unit tests by evolving test code via genetic algorithms to maximize coverage. Tests are represented as chromosomes of object and message statements. The genetic algorithm selects tests based on coverage, combines tests through crossover, and replaces tests in the population over generations to find optimal test sequences. Future work includes improving path exploration and comparing with other test generation tools.
Threaded-Execution and CPS Provide Smooth Switching Between Execution ModesESUG
Threaded execution and continuation-passing style (CPS) allow for smooth switching between execution modes in Zag Smalltalk. Threaded execution interprets code as a sequence of addresses like bytecode but is 2.3-4.7 times faster, while CPS passes continuations explicitly like in functional languages and is 3-5 times faster than bytecode. Both approaches allow fallback to debugging. The implementation shares context and stack between modes to easily switch with proper object structures.
Exploring GitHub Actions through EGAD: An Experience ReportESUG
This document summarizes an experience report on exploring GitHub Actions through EGAD, a tool for GitHub Action analysis. It discusses three key lessons learned: 1) Composing a story by documenting tasks and linking documentation to code, 2) Navigating custom views to conduct research, and 3) Supporting onboarding of researchers by assigning mentors, scheduling meetings, and encouraging use of resources. EGAD takes workflow YAML files, wraps them in a domain model to provide context, and allows inspecting examples to fully explore the GitHub Actions domain model.
Pharo: a reflective language A first systematic analysis of reflective APIsESUG
This document analyzes the reflective features and APIs in Pharo, a reflective programming language. It presents a catalog of Pharo's reflective APIs and analyzes how they relate to metaobjects. The analysis highlights areas for potential improvement, such as providing solutions for intercession on state reads/writes and addressing constraints when changing an object's class. The document contributes to understanding Pharo's reflective design and its evolution over time.
The document discusses garbage collector tuning for applications with pathological allocation patterns. It begins by explaining the motivation and issues caused by pathological patterns, such as applications taking over an hour and a half to run. It then provides an overview of garbage collection and how allocation patterns can impact performance. The document dives into two specific tuning techniques - increasing the full GC threshold to prevent premature full GCs from being triggered, and increasing the tenuring threshold to avoid large objects residing in the remembered set and slowing down scavenges. These tunings resulted in significant performance improvements for the sample DataFrame application, reducing the run time from over an hour and a half to around seven minutes.
Improving Performance Through Object Lifetime Profiling: the DataFrame CaseESUG
This document discusses improving garbage collection performance in Pharo through object lifetime profiling. It presents Illimani, a lifetime profiler developed for Pharo. Illimani was used to profile the lifetimes of objects created when loading a large DataFrame. The profiling revealed that most objects had short lifetimes, suggesting the garbage collector could be tuned. Tuning the garbage collector parameters based on the lifetime profiles improved the performance of loading the DataFrame.
This document discusses the past, present, and future of Pharo DataFrames. It began as a student project but has evolved into a mature project with dedicated engineers, improving performance and adding functionality. Future plans include further performance enhancements, adding more functionality, better integration with other Pharo projects, and support for big data. Evaluation of DataFrames is also planned.
This document discusses issues with thisContext in the Pharo debugger not correctly representing the execution context and being the DoIt context instead. This was fixed in Pharo12 by making thisContext a variable object that is wrapped in a DoItVariable, so the debugger context is used. When inspecting or doing DoIt, the doIt Variable is pushed and read to provide the proper execution context.
This document proposes using websockets to display fencing scores and a chronometer from an arena server to mobile phones over the internet in real-time. It includes links to video examples of a chronometer display and photos from fencing competitions.
ShowUs: PharoJS.org Develop in Pharo, Run on JavaScriptESUG
This document discusses PharoJS, which allows developers to develop applications in Pharo and then export them to run as JavaScript applications. PharoJS enables 100% of Pharo code to be executed during development, and then 100% of that same code is exported to JavaScript to be executed in production. The document also briefly mentions deployment options for exported PharoJS applications like GitHub Pages and GitHub Actions.
The document contains testimonials from participants of the Pharo MOOC praising its effectiveness at teaching object-oriented design. It also announces an upcoming advanced design MOOC that will have over 60 lectures, slides, videos and an exercise booklet. Finally, it provides links to the course websites and encourages people to stay tuned for the new MOOC.
A New Architecture Reconciling Refactorings and TransformationsESUG
This document discusses reconciling refactorings and transformations in software engineering. It proposes a new architecture where refactorings decorate transformations by checking preconditions and composing multiple transformations. Refactorings ensure transformations are applied safely while transformations focus on model changes. Open questions remain around precondition handling and composition semantics. The goals are to reduce duplication, support custom refactorings/transformations, and provide a modern driver-based user interface.
Dive into the realm of operating systems (OS) with Pravash Chandra Das, a seasoned Digital Forensic Analyst, as your guide. 🚀 This comprehensive presentation illuminates the core concepts, types, and evolution of OS, essential for understanding modern computing landscapes.
Beginning with the foundational definition, Das clarifies the pivotal role of OS as system software orchestrating hardware resources, software applications, and user interactions. Through succinct descriptions, he delineates the diverse types of OS, from single-user, single-task environments like early MS-DOS iterations, to multi-user, multi-tasking systems exemplified by modern Linux distributions.
Crucial components like the kernel and shell are dissected, highlighting their indispensable functions in resource management and user interface interaction. Das elucidates how the kernel acts as the central nervous system, orchestrating process scheduling, memory allocation, and device management. Meanwhile, the shell serves as the gateway for user commands, bridging the gap between human input and machine execution. 💻
The narrative then shifts to a captivating exploration of prominent desktop OSs, Windows, macOS, and Linux. Windows, with its globally ubiquitous presence and user-friendly interface, emerges as a cornerstone in personal computing history. macOS, lauded for its sleek design and seamless integration with Apple's ecosystem, stands as a beacon of stability and creativity. Linux, an open-source marvel, offers unparalleled flexibility and security, revolutionizing the computing landscape. 🖥️
Moving to the realm of mobile devices, Das unravels the dominance of Android and iOS. Android's open-source ethos fosters a vibrant ecosystem of customization and innovation, while iOS boasts a seamless user experience and robust security infrastructure. Meanwhile, discontinued platforms like Symbian and Palm OS evoke nostalgia for their pioneering roles in the smartphone revolution.
The journey concludes with a reflection on the ever-evolving landscape of OS, underscored by the emergence of real-time operating systems (RTOS) and the persistent quest for innovation and efficiency. As technology continues to shape our world, understanding the foundations and evolution of operating systems remains paramount. Join Pravash Chandra Das on this illuminating journey through the heart of computing. 🌟
Letter and Document Automation for Bonterra Impact Management (fka Social Sol...Jeffrey Haguewood
Sidekick Solutions uses Bonterra Impact Management (fka Social Solutions Apricot) and automation solutions to integrate data for business workflows.
We believe integration and automation are essential to user experience and the promise of efficient work through technology. Automation is the critical ingredient to realizing that full vision. We develop integration products and services for Bonterra Case Management software to support the deployment of automations for a variety of use cases.
This video focuses on automated letter generation for Bonterra Impact Management using Google Workspace or Microsoft 365.
Interested in deploying letter generation automations for Bonterra Impact Management? Contact us at sales@sidekicksolutionsllc.com to discuss next steps.
HCL Notes und Domino Lizenzkostenreduzierung in der Welt von DLAUpanagenda
Webinar Recording: https://www.panagenda.com/webinars/hcl-notes-und-domino-lizenzkostenreduzierung-in-der-welt-von-dlau/
DLAU und die Lizenzen nach dem CCB- und CCX-Modell sind für viele in der HCL-Community seit letztem Jahr ein heißes Thema. Als Notes- oder Domino-Kunde haben Sie vielleicht mit unerwartet hohen Benutzerzahlen und Lizenzgebühren zu kämpfen. Sie fragen sich vielleicht, wie diese neue Art der Lizenzierung funktioniert und welchen Nutzen sie Ihnen bringt. Vor allem wollen Sie sicherlich Ihr Budget einhalten und Kosten sparen, wo immer möglich. Das verstehen wir und wir möchten Ihnen dabei helfen!
Wir erklären Ihnen, wie Sie häufige Konfigurationsprobleme lösen können, die dazu führen können, dass mehr Benutzer gezählt werden als nötig, und wie Sie überflüssige oder ungenutzte Konten identifizieren und entfernen können, um Geld zu sparen. Es gibt auch einige Ansätze, die zu unnötigen Ausgaben führen können, z. B. wenn ein Personendokument anstelle eines Mail-Ins für geteilte Mailboxen verwendet wird. Wir zeigen Ihnen solche Fälle und deren Lösungen. Und natürlich erklären wir Ihnen das neue Lizenzmodell.
Nehmen Sie an diesem Webinar teil, bei dem HCL-Ambassador Marc Thomas und Gastredner Franz Walder Ihnen diese neue Welt näherbringen. Es vermittelt Ihnen die Tools und das Know-how, um den Überblick zu bewahren. Sie werden in der Lage sein, Ihre Kosten durch eine optimierte Domino-Konfiguration zu reduzieren und auch in Zukunft gering zu halten.
Diese Themen werden behandelt
- Reduzierung der Lizenzkosten durch Auffinden und Beheben von Fehlkonfigurationen und überflüssigen Konten
- Wie funktionieren CCB- und CCX-Lizenzen wirklich?
- Verstehen des DLAU-Tools und wie man es am besten nutzt
- Tipps für häufige Problembereiche, wie z. B. Team-Postfächer, Funktions-/Testbenutzer usw.
- Praxisbeispiele und Best Practices zum sofortigen Umsetzen
Have you ever been confused by the myriad of choices offered by AWS for hosting a website or an API?
Lambda, Elastic Beanstalk, Lightsail, Amplify, S3 (and more!) can each host websites + APIs. But which one should we choose?
Which one is cheapest? Which one is fastest? Which one will scale to meet our needs?
Join me in this session as we dive into each AWS hosting service to determine which one is best for your scenario and explain why!
Generating privacy-protected synthetic data using Secludy and MilvusZilliz
During this demo, the founders of Secludy will demonstrate how their system utilizes Milvus to store and manipulate embeddings for generating privacy-protected synthetic data. Their approach not only maintains the confidentiality of the original data but also enhances the utility and scalability of LLMs under privacy constraints. Attendees, including machine learning engineers, data scientists, and data managers, will witness first-hand how Secludy's integration with Milvus empowers organizations to harness the power of LLMs securely and efficiently.
Ocean lotus Threat actors project by John Sitima 2024 (1).pptxSitimaJohn
Ocean Lotus cyber threat actors represent a sophisticated, persistent, and politically motivated group that poses a significant risk to organizations and individuals in the Southeast Asian region. Their continuous evolution and adaptability underscore the need for robust cybersecurity measures and international cooperation to identify and mitigate the threats posed by such advanced persistent threat groups.
Taking AI to the Next Level in Manufacturing.pdfssuserfac0301
Read Taking AI to the Next Level in Manufacturing to gain insights on AI adoption in the manufacturing industry, such as:
1. How quickly AI is being implemented in manufacturing.
2. Which barriers stand in the way of AI adoption.
3. How data quality and governance form the backbone of AI.
4. Organizational processes and structures that may inhibit effective AI adoption.
6. Ideas and approaches to help build your organization's AI strategy.
Building Production Ready Search Pipelines with Spark and MilvusZilliz
Spark is the widely used ETL tool for processing, indexing and ingesting data to serving stack for search. Milvus is the production-ready open-source vector database. In this talk we will show how to use Spark to process unstructured data to extract vector representations, and push the vectors to Milvus vector database for search serving.
Skybuffer SAM4U tool for SAP license adoptionTatiana Kojar
Manage and optimize your license adoption and consumption with SAM4U, an SAP free customer software asset management tool.
SAM4U, an SAP complimentary software asset management tool for customers, delivers a detailed and well-structured overview of license inventory and usage with a user-friendly interface. We offer a hosted, cost-effective, and performance-optimized SAM4U setup in the Skybuffer Cloud environment. You retain ownership of the system and data, while we manage the ABAP 7.58 infrastructure, ensuring fixed Total Cost of Ownership (TCO) and exceptional services through the SAP Fiori interface.
Monitoring and Managing Anomaly Detection on OpenShift.pdfTosin Akinosho
Monitoring and Managing Anomaly Detection on OpenShift
Overview
Dive into the world of anomaly detection on edge devices with our comprehensive hands-on tutorial. This SlideShare presentation will guide you through the entire process, from data collection and model training to edge deployment and real-time monitoring. Perfect for those looking to implement robust anomaly detection systems on resource-constrained IoT/edge devices.
Key Topics Covered
1. Introduction to Anomaly Detection
- Understand the fundamentals of anomaly detection and its importance in identifying unusual behavior or failures in systems.
2. Understanding Edge (IoT)
- Learn about edge computing and IoT, and how they enable real-time data processing and decision-making at the source.
3. What is ArgoCD?
- Discover ArgoCD, a declarative, GitOps continuous delivery tool for Kubernetes, and its role in deploying applications on edge devices.
4. Deployment Using ArgoCD for Edge Devices
- Step-by-step guide on deploying anomaly detection models on edge devices using ArgoCD.
5. Introduction to Apache Kafka and S3
- Explore Apache Kafka for real-time data streaming and Amazon S3 for scalable storage solutions.
6. Viewing Kafka Messages in the Data Lake
- Learn how to view and analyze Kafka messages stored in a data lake for better insights.
7. What is Prometheus?
- Get to know Prometheus, an open-source monitoring and alerting toolkit, and its application in monitoring edge devices.
8. Monitoring Application Metrics with Prometheus
- Detailed instructions on setting up Prometheus to monitor the performance and health of your anomaly detection system.
9. What is Camel K?
- Introduction to Camel K, a lightweight integration framework built on Apache Camel, designed for Kubernetes.
10. Configuring Camel K Integrations for Data Pipelines
- Learn how to configure Camel K for seamless data pipeline integrations in your anomaly detection workflow.
11. What is a Jupyter Notebook?
- Overview of Jupyter Notebooks, an open-source web application for creating and sharing documents with live code, equations, visualizations, and narrative text.
12. Jupyter Notebooks with Code Examples
- Hands-on examples and code snippets in Jupyter Notebooks to help you implement and test anomaly detection models.
Fueling AI with Great Data with Airbyte WebinarZilliz
This talk will focus on how to collect data from a variety of sources, leveraging this data for RAG and other GenAI use cases, and finally charting your course to productionalization.
Best 20 SEO Techniques To Improve Website Visibility In SERPPixlogix Infotech
Boost your website's visibility with proven SEO techniques! Our latest blog dives into essential strategies to enhance your online presence, increase traffic, and rank higher on search engines. From keyword optimization to quality content creation, learn how to make your site stand out in the crowded digital landscape. Discover actionable tips and expert insights to elevate your SEO game.
5th LF Energy Power Grid Model Meet-up SlidesDanBrown980551
5th Power Grid Model Meet-up
It is with great pleasure that we extend to you an invitation to the 5th Power Grid Model Meet-up, scheduled for 6th June 2024. This event will adopt a hybrid format, allowing participants to join us either through an online Mircosoft Teams session or in person at TU/e located at Den Dolech 2, Eindhoven, Netherlands. The meet-up will be hosted by Eindhoven University of Technology (TU/e), a research university specializing in engineering science & technology.
Power Grid Model
The global energy transition is placing new and unprecedented demands on Distribution System Operators (DSOs). Alongside upgrades to grid capacity, processes such as digitization, capacity optimization, and congestion management are becoming vital for delivering reliable services.
Power Grid Model is an open source project from Linux Foundation Energy and provides a calculation engine that is increasingly essential for DSOs. It offers a standards-based foundation enabling real-time power systems analysis, simulations of electrical power grids, and sophisticated what-if analysis. In addition, it enables in-depth studies and analysis of the electrical power grid’s behavior and performance. This comprehensive model incorporates essential factors such as power generation capacity, electrical losses, voltage levels, power flows, and system stability.
Power Grid Model is currently being applied in a wide variety of use cases, including grid planning, expansion, reliability, and congestion studies. It can also help in analyzing the impact of renewable energy integration, assessing the effects of disturbances or faults, and developing strategies for grid control and optimization.
What to expect
For the upcoming meetup we are organizing, we have an exciting lineup of activities planned:
-Insightful presentations covering two practical applications of the Power Grid Model.
-An update on the latest advancements in Power Grid -Model technology during the first and second quarters of 2024.
-An interactive brainstorming session to discuss and propose new feature requests.
-An opportunity to connect with fellow Power Grid Model enthusiasts and users.
How to Interpret Trends in the Kalyan Rajdhani Mix Chart.pdfChart Kalyan
A Mix Chart displays historical data of numbers in a graphical or tabular form. The Kalyan Rajdhani Mix Chart specifically shows the results of a sequence of numbers over different periods.