Study of the Methods for Decision Making in the Monitoring and Control of Production in the Ecuadorian Pharmaceutical Industries for Project use using Comprehensive Control Panel and Business Architecture
This document discusses methods for decision making in monitoring and controlling production processes in Ecuadorian pharmaceutical industries. It conducted a survey of 16 pharmaceutical companies producing injectables and tablets. The survey aimed to understand the current situation regarding monitoring and control applied in production processes. It found that companies make decisions based on experience or spreadsheets, with few using computer tools. It proposed using a balanced scorecard and business architecture approach to organize information and processes to improve decision making, reduce risks, and increase productivity and profitability. The project aims to help pharmaceutical industries in Ecuador improve production monitoring and control for quality medicines.
Performance metrics are an essential element of the management review process.
Quality metrics may include elements such as customer satisfaction, supplier performance, manufacturing defects, complaints, cycle times and many other internal or external processes.
This presentation provides a framework for establishing right quality indicators for evaluating the performance of the quality system.
Pharmaceutical 6 Sigma and QbD May 2005 Ball State UniversityAjaz Hussain
Pharmaceutical product and process quality – what is the current “sigma”?
Challenges in moving towards “6-sigma” levels?
What are the steps necessary for the pharmaceutical continuous improvement journey in the 21st Century?
Statistical quality control irfan bashir kardaash - copyIRFAN BASHIR
This document provides an overview of statistical quality control and control charts. It discusses how statistical quality control methods were pioneered in the 1920s and helped improve quality for US industry. Control charts are introduced as a key tool for monitoring processes and detecting when processes go out of control due to assignable causes. The document also discusses advantages of statistical quality control over 100% inspection and different types of quality control including process control and product or lot control.
This document provides an overview of statistical quality control. It discusses Walter Shewhart, considered the father of statistical quality control, and his development of statistical procedures and charts for controlling manufacturing processes. It also covers W. Edwards Deming and his influential 14 points program for quality management, which emphasized process improvement over inspection and the importance of management commitment to quality. The document defines statistical process control and its goal of monitoring production through various stages to help identify out-of-control processes. It notes the increased emphasis on quality control since World War II.
The document discusses a framework for transferring technology to emerging markets to satisfy new process validation guidance. It provides an overview of the new FDA process validation guidance, comparing it to the previous 1987 guidance. Key changes include a focus on scientific evidence throughout the product lifecycle rather than just documentation. The new guidance also defines process validation as having three stages: process design, process qualification, and continued process monitoring. The document then discusses considerations for technology transfer and process validation in emerging markets like China based on the new FDA guidance.
Aligning data life cycle with qb d risk management principle across the produ...SANDEEP DIWAKER
Dear all,
Herewith sharing the presentation on “Aligning Data Life Cycle with QbD Risk Management Principle across the product life cycle” session conducted in Biotrains event on “Data Integrity”
This document provides an overview of quality management review including definitions, purposes, and tools. It discusses that quality management reviews are conducted regularly according to ISO 9001 standards to evaluate the quality management system. The review assesses adequacy, suitability, and effectiveness of the system. Several quality management tools are also introduced, including check sheets, control charts, Pareto charts, scatter plots, and Ishikawa diagrams.
Performance metrics are an essential element of the management review process.
Quality metrics may include elements such as customer satisfaction, supplier performance, manufacturing defects, complaints, cycle times and many other internal or external processes.
This presentation provides a framework for establishing right quality indicators for evaluating the performance of the quality system.
Pharmaceutical 6 Sigma and QbD May 2005 Ball State UniversityAjaz Hussain
Pharmaceutical product and process quality – what is the current “sigma”?
Challenges in moving towards “6-sigma” levels?
What are the steps necessary for the pharmaceutical continuous improvement journey in the 21st Century?
Statistical quality control irfan bashir kardaash - copyIRFAN BASHIR
This document provides an overview of statistical quality control and control charts. It discusses how statistical quality control methods were pioneered in the 1920s and helped improve quality for US industry. Control charts are introduced as a key tool for monitoring processes and detecting when processes go out of control due to assignable causes. The document also discusses advantages of statistical quality control over 100% inspection and different types of quality control including process control and product or lot control.
This document provides an overview of statistical quality control. It discusses Walter Shewhart, considered the father of statistical quality control, and his development of statistical procedures and charts for controlling manufacturing processes. It also covers W. Edwards Deming and his influential 14 points program for quality management, which emphasized process improvement over inspection and the importance of management commitment to quality. The document defines statistical process control and its goal of monitoring production through various stages to help identify out-of-control processes. It notes the increased emphasis on quality control since World War II.
The document discusses a framework for transferring technology to emerging markets to satisfy new process validation guidance. It provides an overview of the new FDA process validation guidance, comparing it to the previous 1987 guidance. Key changes include a focus on scientific evidence throughout the product lifecycle rather than just documentation. The new guidance also defines process validation as having three stages: process design, process qualification, and continued process monitoring. The document then discusses considerations for technology transfer and process validation in emerging markets like China based on the new FDA guidance.
Aligning data life cycle with qb d risk management principle across the produ...SANDEEP DIWAKER
Dear all,
Herewith sharing the presentation on “Aligning Data Life Cycle with QbD Risk Management Principle across the product life cycle” session conducted in Biotrains event on “Data Integrity”
This document provides an overview of quality management review including definitions, purposes, and tools. It discusses that quality management reviews are conducted regularly according to ISO 9001 standards to evaluate the quality management system. The review assesses adequacy, suitability, and effectiveness of the system. Several quality management tools are also introduced, including check sheets, control charts, Pareto charts, scatter plots, and Ishikawa diagrams.
The document discusses risk management for pharmaceutical projects. It begins by outlining the characteristics of the pharmaceutical industry and drug development process. The drug development process takes an average of 10 years and $2.6 billion to develop a new drug. The presentation then covers risk management processes, tools and techniques for identifying, analyzing, and responding to risks in drug development projects. A case study on risk assessment for product development is presented to demonstrate how to evaluate risks and prioritize mitigation actions.
CAPA: Using Risk-Based Decision-Making Toward ClosureApril Bright
Implementing a risk‐based CAPA process within a QMS is a necessity in the improvement of controls aligned with product and process non-conformances, adverse events, audit findings, complaints, etc. Making decisions concerning scope and extent about these “defectives” is a modern and cost-saving approach to improvement and compliance. Every non-conformity does not force you to open a corrective action. While almost every problematic issue needs at least a correction, the biggest payback is to use corrective actions on systemically-driven problems that are repetitive and recurring.
Applying the methods of determining risk to the device’s complete life cycle will give your company a complete look at all of the device’s risks—including those relative to processes. Manufacturers should be able to justify that they have reduced the risks as far as possible as part of their risk management plan and ongoing corrective and preventive actions.
A proper technology transfer (TT) is both essential and important to drug discovery and development for new medicinal products. It is also required to upgrade drug quality planned during research development and to final product during manufacturing as well as to guarantee that stable quality is transferred
Course Objectives:
How does industry use Metrics?
FDA Challenges and Requirements and Use of Quality Metrics
Complexities of Implementation (Industry Feedback)
What does it all mean?
Key in Risk identification – systematic use of information to identify potential sources of harm (hazards)
referring to the risk question or problem description.
Enables the detection of potential problems as early as possible to plan corrective and preventive
actions
Provides indication that controls are losing effectiveness Important in achieving problem resolution and problem prevention
Another important concept of modern quality systems is the use of trending to examine processes as a whole.
Driving wrong behaviors and unintended consequence
• Establishing excessive or overly complex metrics
Comparing data that is not consistently defined or comparison of single data values
Using metrics as a quality “surrogate”
Quality by design in pharmaceutical developmentManish Rajput
This document discusses the concept of Quality by Design (QbD) in pharmaceutical development. It provides background on QbD and outlines its key aspects, including defining target product profiles, critical quality attributes, risk assessment, design space, control strategy, and life cycle management. The benefits of QbD for industry and regulators are described. Traditional and QbD approaches to pharmaceutical development are compared. Tools used in QbD such as design of experiments, risk assessment methodologies, and process analytical technology are also summarized. Finally, an example application of QbD principles to influenza vaccine development is presented.
Product Complaints: Complaint Handling from Intake to ClosureGRCTS
Overview :
An effective complaint handling system is an extremely important part of any quality system whether you are a medical device or pharmaceutical manufacturer. Manufacturers should understand that any complaint received on a product shall be evaluated and, if necessary, thoroughly investigated and analyzed, and corrective action shall be taken. Manufacturers must ensure that they have a well-designed system to address complaints related to their products. Components of a well-designed system include: process/procedure, trained personnel, and proper record keeping. Complaint handling is no easy task. Management might overlook the importance of customer feedback and be unable to capture all complaints coming from disparate sources. Plus, the additional regulatory reporting requirement related to adverse events may seem overly burdensome to device makers in particular. A strategic risk-based methodology can help streamline the complaint-handling process in medical device manufacturing.
This document discusses quality risk management standard operating procedures (SOPs). It provides links to additional quality management resources and outlines the contents of a quality risk management SOP, including quality risk management principles, tools like check sheets and control charts, and ensuring focus on protecting patients.
This document discusses technology transfer in the pharmaceutical industry. It begins with an introduction and overview, then discusses the basic concepts and stages of technology transfer. The key stages are research, development, and production. Technology transfer is important for upgrading drug quality during manufacturing and ensuring quality is maintained between different production sites. Effective communication between all stakeholders is key to the successful transfer of technology.
The presentation discusses the current state of quality management in the pharmaceutical industry and a proposed future "desired state" based on a risk-based, science-driven approach. It highlights guidelines from the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) including ICH Q6A on specifications and ICH Q8 on pharmaceutical development. The desired state focuses on process understanding, continuous monitoring and improvement rather than just documentation and testing to ensure consistent product quality.
Maximizing Use of Your Supplier Scorecard - OMTEC 2018April Bright
Supplier scorecards provide a comparative look at suppliers and a heightened understanding of internal challenges within your organizations. Orthopaedic device companies rely on scorecards to monitor the performance of suppliers that are an extension of their own operations. The right elements in the scorecard (e.g. weighted factors of quality, delivery, cost, responsiveness, SCAR, CAPA, etc.) will strengthen your confidence, control and relationship with your suppliers while simultaneously providing essential indicators to drive positive change.
Technology transfer is the process of sharing manufacturing knowledge, technologies, and processes between organizations. In the pharmaceutical industry, it refers to transferring a drug product from development to commercial manufacturing. Effective technology transfer requires careful planning, documentation exchange, verification of analytical methods, small-scale testing, and ensuring manufacturing processes are well-understood before full-scale production. It is a critical step to successful commercialization and requires consideration of regulatory requirements, personnel, manufacturing changes, and validation approaches.
This document provides an introduction to quality concepts, including ISO 9001 standards, processes, quality control, quality assurance, and total quality management. It discusses how focusing on quality can help businesses stay operational by exceeding customer expectations and maintaining continuous improvement. Key aspects that help ensure quality like process control and Deming's management obligations are also summarized. The document emphasizes that quality must be a priority from the planning stage and should engage all employees to best serve customers.
Winning Strategies for Tech Transfer ProjectsAnthony Grenier
This document discusses technology transfer strategies for moving manufacturing processes to new facilities. It outlines key drivers for technology transfer like capacity needs and cost reductions. The technology transfer process involves defining the product and process, assessing fit at the new site, planning the transfer, and conducting readiness checks. A case study describes an Indian CMO facility set up for microbial biotherapeutic production using disposable and reusable equipment across upstream and downstream processing. The facility utilizes buffer preparation and storage systems to support purification operations.
To Analyze the Use of Statistical Tool/S for Cost Effectiveness and Quality o...iosrjce
Companies can lose money because they fail to use significant opportunities to improve product
quality as well as product cost. In order to survive in a competitive market, reduce cost of product by improving
the quality and productivity of product is must for any company.
The objective of this study is to provide system/instructions and methodology to reduce cost of product by
implementing statistical tools in local plastic injection molding company. Injection molding Company deployed
some part of the “Seven Basic Tools” to improve the quality of the product used by our society and reduce cost
of the product. Companies may reluctant to their quality status and customer satisfactory status without
implementing any helping tool which may reduce cost by identifying and decreasing number of defects and
consequently improving product quality and productivity of the system/process. Statistical techniques like
“Seven Basic Statistical Tools” (SPC) provides a very valuable and cost effective way to meet these objectives.
The principle aim of this study is to train quality personnel that how to use these SPC tools and exploit these
data in Pareto analysis, control Chart, Cause & Effect Diagram and histogram analysis. The causes of nonconformity
and root causes of quality problems were specified and possible remedies were proposed to
organization to overcome their problems. Some significant Improvement was also observed after SPC
implementation in Process potential capability (Cp), Process Actual Capability (Cpk) and Defective parts per
million (DPM)
Quality management systems - INDUSTRIAL PHARMACY llJafarali Masi
syllabus
Quality management & Certifications: Concept of Quality, Total Quality Management, Quality by Design (QbD), Six Sigma concept, Out of Specifications (OOS), Change control, Introduction to ISO 9000 series of quality systems standards, ISO 14000, NABL, GLP
The document discusses Process Analytical Technology (PAT), which is defined as a system for designing, analyzing, and controlling manufacturing processes through measurements of critical quality attributes during processing. PAT aims to ensure final product quality by building quality into products through enhanced process understanding and control. The key elements of a PAT framework include process understanding, principles and tools like multivariate analysis, process analyzers, process controls, continuous improvement, and risk-based approaches. PAT offers benefits like increased flexibility, reduced costs and improved yields.
Pharmaceutical Technology Transfer Best PracticesAnthony Grenier
Key Takeaways from the Technology Transfer Guidelines
• Standardize checklist for transferring product development, process development, and analytical method development knowledge
• Requirements are summarized in key deliverables and reports
The document discusses Quality by Design (QbD), which is defined as using a multidisciplinary team to simultaneously conduct conceptual thinking, product design, and production planning. QbD emphasizes understanding how product and process variables impact quality through science and risk management. It involves defining quality targets, critical quality attributes, and linking these to raw materials and processes. Teams should include specialists from different areas. QbD allows for improved quality, reduced costs and time to market through understanding relationships between inputs and outputs early in development. Implementation requires preparation, training, and overcoming challenges like cultural changes and costs.
Fundamentals of manufacturing excellenceMAHESH BALAN
This document discusses fundamentals of manufacturing excellence. It summarizes that leadership must establish clear goals focused on customers and continuous improvement. World-class manufacturers integrate all elements and break down barriers for effective communication. The organization must understand customers' needs and optimize the system to meet those needs. Customers purchase solutions, not individual functions, so the whole organization must work together toward customer satisfaction.
Tackling the Challanges of Pharma ManufacturingJason Corder
By nature, pharmaceutical manufacturing operations are complex, inefficient, and consequently costly. Due to the inherent complexities, the cost of poor efficiency and its root causes are often not well understood by many manufacturers.
The document discusses risk management for pharmaceutical projects. It begins by outlining the characteristics of the pharmaceutical industry and drug development process. The drug development process takes an average of 10 years and $2.6 billion to develop a new drug. The presentation then covers risk management processes, tools and techniques for identifying, analyzing, and responding to risks in drug development projects. A case study on risk assessment for product development is presented to demonstrate how to evaluate risks and prioritize mitigation actions.
CAPA: Using Risk-Based Decision-Making Toward ClosureApril Bright
Implementing a risk‐based CAPA process within a QMS is a necessity in the improvement of controls aligned with product and process non-conformances, adverse events, audit findings, complaints, etc. Making decisions concerning scope and extent about these “defectives” is a modern and cost-saving approach to improvement and compliance. Every non-conformity does not force you to open a corrective action. While almost every problematic issue needs at least a correction, the biggest payback is to use corrective actions on systemically-driven problems that are repetitive and recurring.
Applying the methods of determining risk to the device’s complete life cycle will give your company a complete look at all of the device’s risks—including those relative to processes. Manufacturers should be able to justify that they have reduced the risks as far as possible as part of their risk management plan and ongoing corrective and preventive actions.
A proper technology transfer (TT) is both essential and important to drug discovery and development for new medicinal products. It is also required to upgrade drug quality planned during research development and to final product during manufacturing as well as to guarantee that stable quality is transferred
Course Objectives:
How does industry use Metrics?
FDA Challenges and Requirements and Use of Quality Metrics
Complexities of Implementation (Industry Feedback)
What does it all mean?
Key in Risk identification – systematic use of information to identify potential sources of harm (hazards)
referring to the risk question or problem description.
Enables the detection of potential problems as early as possible to plan corrective and preventive
actions
Provides indication that controls are losing effectiveness Important in achieving problem resolution and problem prevention
Another important concept of modern quality systems is the use of trending to examine processes as a whole.
Driving wrong behaviors and unintended consequence
• Establishing excessive or overly complex metrics
Comparing data that is not consistently defined or comparison of single data values
Using metrics as a quality “surrogate”
Quality by design in pharmaceutical developmentManish Rajput
This document discusses the concept of Quality by Design (QbD) in pharmaceutical development. It provides background on QbD and outlines its key aspects, including defining target product profiles, critical quality attributes, risk assessment, design space, control strategy, and life cycle management. The benefits of QbD for industry and regulators are described. Traditional and QbD approaches to pharmaceutical development are compared. Tools used in QbD such as design of experiments, risk assessment methodologies, and process analytical technology are also summarized. Finally, an example application of QbD principles to influenza vaccine development is presented.
Product Complaints: Complaint Handling from Intake to ClosureGRCTS
Overview :
An effective complaint handling system is an extremely important part of any quality system whether you are a medical device or pharmaceutical manufacturer. Manufacturers should understand that any complaint received on a product shall be evaluated and, if necessary, thoroughly investigated and analyzed, and corrective action shall be taken. Manufacturers must ensure that they have a well-designed system to address complaints related to their products. Components of a well-designed system include: process/procedure, trained personnel, and proper record keeping. Complaint handling is no easy task. Management might overlook the importance of customer feedback and be unable to capture all complaints coming from disparate sources. Plus, the additional regulatory reporting requirement related to adverse events may seem overly burdensome to device makers in particular. A strategic risk-based methodology can help streamline the complaint-handling process in medical device manufacturing.
This document discusses quality risk management standard operating procedures (SOPs). It provides links to additional quality management resources and outlines the contents of a quality risk management SOP, including quality risk management principles, tools like check sheets and control charts, and ensuring focus on protecting patients.
This document discusses technology transfer in the pharmaceutical industry. It begins with an introduction and overview, then discusses the basic concepts and stages of technology transfer. The key stages are research, development, and production. Technology transfer is important for upgrading drug quality during manufacturing and ensuring quality is maintained between different production sites. Effective communication between all stakeholders is key to the successful transfer of technology.
The presentation discusses the current state of quality management in the pharmaceutical industry and a proposed future "desired state" based on a risk-based, science-driven approach. It highlights guidelines from the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) including ICH Q6A on specifications and ICH Q8 on pharmaceutical development. The desired state focuses on process understanding, continuous monitoring and improvement rather than just documentation and testing to ensure consistent product quality.
Maximizing Use of Your Supplier Scorecard - OMTEC 2018April Bright
Supplier scorecards provide a comparative look at suppliers and a heightened understanding of internal challenges within your organizations. Orthopaedic device companies rely on scorecards to monitor the performance of suppliers that are an extension of their own operations. The right elements in the scorecard (e.g. weighted factors of quality, delivery, cost, responsiveness, SCAR, CAPA, etc.) will strengthen your confidence, control and relationship with your suppliers while simultaneously providing essential indicators to drive positive change.
Technology transfer is the process of sharing manufacturing knowledge, technologies, and processes between organizations. In the pharmaceutical industry, it refers to transferring a drug product from development to commercial manufacturing. Effective technology transfer requires careful planning, documentation exchange, verification of analytical methods, small-scale testing, and ensuring manufacturing processes are well-understood before full-scale production. It is a critical step to successful commercialization and requires consideration of regulatory requirements, personnel, manufacturing changes, and validation approaches.
This document provides an introduction to quality concepts, including ISO 9001 standards, processes, quality control, quality assurance, and total quality management. It discusses how focusing on quality can help businesses stay operational by exceeding customer expectations and maintaining continuous improvement. Key aspects that help ensure quality like process control and Deming's management obligations are also summarized. The document emphasizes that quality must be a priority from the planning stage and should engage all employees to best serve customers.
Winning Strategies for Tech Transfer ProjectsAnthony Grenier
This document discusses technology transfer strategies for moving manufacturing processes to new facilities. It outlines key drivers for technology transfer like capacity needs and cost reductions. The technology transfer process involves defining the product and process, assessing fit at the new site, planning the transfer, and conducting readiness checks. A case study describes an Indian CMO facility set up for microbial biotherapeutic production using disposable and reusable equipment across upstream and downstream processing. The facility utilizes buffer preparation and storage systems to support purification operations.
To Analyze the Use of Statistical Tool/S for Cost Effectiveness and Quality o...iosrjce
Companies can lose money because they fail to use significant opportunities to improve product
quality as well as product cost. In order to survive in a competitive market, reduce cost of product by improving
the quality and productivity of product is must for any company.
The objective of this study is to provide system/instructions and methodology to reduce cost of product by
implementing statistical tools in local plastic injection molding company. Injection molding Company deployed
some part of the “Seven Basic Tools” to improve the quality of the product used by our society and reduce cost
of the product. Companies may reluctant to their quality status and customer satisfactory status without
implementing any helping tool which may reduce cost by identifying and decreasing number of defects and
consequently improving product quality and productivity of the system/process. Statistical techniques like
“Seven Basic Statistical Tools” (SPC) provides a very valuable and cost effective way to meet these objectives.
The principle aim of this study is to train quality personnel that how to use these SPC tools and exploit these
data in Pareto analysis, control Chart, Cause & Effect Diagram and histogram analysis. The causes of nonconformity
and root causes of quality problems were specified and possible remedies were proposed to
organization to overcome their problems. Some significant Improvement was also observed after SPC
implementation in Process potential capability (Cp), Process Actual Capability (Cpk) and Defective parts per
million (DPM)
Quality management systems - INDUSTRIAL PHARMACY llJafarali Masi
syllabus
Quality management & Certifications: Concept of Quality, Total Quality Management, Quality by Design (QbD), Six Sigma concept, Out of Specifications (OOS), Change control, Introduction to ISO 9000 series of quality systems standards, ISO 14000, NABL, GLP
The document discusses Process Analytical Technology (PAT), which is defined as a system for designing, analyzing, and controlling manufacturing processes through measurements of critical quality attributes during processing. PAT aims to ensure final product quality by building quality into products through enhanced process understanding and control. The key elements of a PAT framework include process understanding, principles and tools like multivariate analysis, process analyzers, process controls, continuous improvement, and risk-based approaches. PAT offers benefits like increased flexibility, reduced costs and improved yields.
Pharmaceutical Technology Transfer Best PracticesAnthony Grenier
Key Takeaways from the Technology Transfer Guidelines
• Standardize checklist for transferring product development, process development, and analytical method development knowledge
• Requirements are summarized in key deliverables and reports
The document discusses Quality by Design (QbD), which is defined as using a multidisciplinary team to simultaneously conduct conceptual thinking, product design, and production planning. QbD emphasizes understanding how product and process variables impact quality through science and risk management. It involves defining quality targets, critical quality attributes, and linking these to raw materials and processes. Teams should include specialists from different areas. QbD allows for improved quality, reduced costs and time to market through understanding relationships between inputs and outputs early in development. Implementation requires preparation, training, and overcoming challenges like cultural changes and costs.
Similar to Study of the Methods for Decision Making in the Monitoring and Control of Production in the Ecuadorian Pharmaceutical Industries for Project use using Comprehensive Control Panel and Business Architecture
Fundamentals of manufacturing excellenceMAHESH BALAN
This document discusses fundamentals of manufacturing excellence. It summarizes that leadership must establish clear goals focused on customers and continuous improvement. World-class manufacturers integrate all elements and break down barriers for effective communication. The organization must understand customers' needs and optimize the system to meet those needs. Customers purchase solutions, not individual functions, so the whole organization must work together toward customer satisfaction.
Tackling the Challanges of Pharma ManufacturingJason Corder
By nature, pharmaceutical manufacturing operations are complex, inefficient, and consequently costly. Due to the inherent complexities, the cost of poor efficiency and its root causes are often not well understood by many manufacturers.
Scenario A specialty memory chip manufacturer is located in South.docxkenjordan97598
Here are three strategic goals that align with the vision and mission statements:
1. Improve quality of care by investing in advanced medical technology and equipment. This supports the mission of providing quality services and the vision of becoming the leading healthcare provider in the region.
2. Expand patient services to include primary care, dental, behavioral health and community outreach programs. This will help achieve the mission of educating the public and the vision of growing the facility over time.
3. Develop strategic partnerships with insurance companies and government organizations to increase patient volume and ensure financial sustainability. This supports both the mission of serving the local community and the vision of a larger, more profitable facility in the long run.
Total Quality Management (TQM) is a management approach focused on customer satisfaction through processes involving all employees. The key principles of TQM include being customer-focused, using a process-centered and integrated systems approach, strategic planning, continual improvement, and fact-based decision making. Achieving TQM requires training all employees, removing barriers to quality work, and instituting leadership to help employees improve.
Week 1 Lecture The Nature of Business ResearchBusiness researc.docxkdennis3
Week 1 Lecture
The Nature of Business Research
Business research covers a wide range of phenomena. For managers, the purpose of research is to provide knowledge regarding the organization, the market, the economy, or another area of uncertainty. A financial manager may ask, “Will the environment for long-term financing be better two years from now?†A personnel manager may ask, “What kind of training is necessary for production employees?†or “What is the reason for the company’s high employee turnover?†A marketing manager may ask, “How can I monitor my retail sales and retail trade activities?†Each of these questions requires information about how the environment, employees, customers, or the economy will respond to executives’ decisions. Research is one of the principal tools for answering these practical questions.
Business research is the application of the scientific method in searching for the truth about business phenomena. These activities include defining business opportunities and problems, generating and evaluating alternative courses of action, and monitoring employee and organizational performance. Business research is more than conducting surveys.6 This process includes idea and theory development, problem definition, searching for and collecting information, analyzing data, and communicating the findings and their implications.
Applied business research is conducted to address a specific business decision for a specific firm or organization. The opening vignette describes a situation in which ESPN used applied research to decide how to best create knowledge of its sports fans and their preferences. Basic business research (sometimes referred to as pure research) is conducted without a specific decision in mind, and it usually does not address the needs of a specific organization.
All research, whether basic or applied, involves the scientific method. The scientific method is the way researchers go about using knowledge and evidence to reach objective conclusions about the real world. The scientific method is the same in social sciences, such as business, as in physical sciences, such as physics. In this case, it is the way we come to understand business phenomena.
A firm can be production-oriented. A production-oriented firm prioritizes the efficiency and effectiveness of production processes in making decisions. Here, research providing input from workers, engineers, finance, and accounting becomes important as the firm seeks to drive costs down. Production-oriented firms are usually very large firms manufacturing products in very large quantities. The third orientation is marketing- oriented, which focuses more on how the firm provides value to customers than on the physical product or production process. With a marketing-oriented organization the majority of research focuses on the customer. Research addressing consumer desires, beliefs, and attitudes becomes essential.
Diagnosing Opportunities: After a.
Connie FarrisProject Performance and Quality Assurance(M.docxmargaretr5
This document discusses quality management strategies for Medical Needs, a company opening locations in Memphis and Nashville to provide medical devices. It outlines a quality management plan involving quality planning, improvement, control, and assurance. Quality dimensions and criteria are identified to measure performance, features, reliability, conformity, durability, serviceability, aesthetics, and perception. The costs of quality include costs of non-conformance from fixing issues and costs of conformance from preventing issues. Lean and ISO quality management techniques will be implemented to ensure quality standards and continual improvement.
Strategic Plan Part 3
By: Christopher Gilbert
BUS/475
Instructor: Dr. Steve Verrone
June 20, 2016
STRATEGIC PLAN PART 3
STRATEGIC PLAN PART 3
1
STRATEGIC OBJECTIVES SUMMARY (BALANCED SCORECARD).
STRATEGY
GOAL- What we want to accomplish
OBJECTIVES- How we are going to accomplish the goal
MEASURE
TARGET
SHAREHOLDER VALUE OR FINANCIAL PERSPECTIVE
Ensure financial benefits are maximized through smart and transparent financial systems.
Allocate budget to support business goals and objectives.
Provide investors with value- relevant information.
Increase market share which will improve our competitive position which will lead to sustainable profitability.
Stay relevant through innovation, respond to customers fast enough and use their ideas, buy off competitors and increase flexibility in operations.
Percentage of total market in the business printing sector
70%
Demonstrate cost savings in the organization as a result of business processes being streamlined.
Use process value analysis on all change initiatives in the organization.
Percentage of change initiatives that produced cost savings in the organization.
75%
PROCESS OR INTERNAL OPERATIONS PERSPECTIVE
Implement strategies to maximize resources and infrastructure present in Neon Software, Inc.’s facilities.
Make use of creativity and innovation in order to improve internal processes and keeps the business progressing.
Ensure high utilization of company facilities.
Improve process delivery
Create business project management process
The process is implemented in full.
PASS/ FAIL
Ensure effective implementation of initiatives
Initiative delivered project goals
Percentage of goals met
90%
Initiative delivered on time
Percentage of initiatives delivered on time
90%
Initiative delivered on budget
Percentage of initiatives delivered on budget
90%
CUSTOMER VALUE PERSPECTIVE
Maximize customer collaboration in order to identify and understand customer needs and expectations.
Deliver timely, accurate, and high-quality services and products to increase value and achieve customer satisfaction.
Products offered by Neon Software, Inc. to be affordable with the firm acting as a market leader.
Identify customer needs and inefficiencies and implement relevant solutions.
Map existing business processes
Number of business processes mapped
4
Facilitate the management of change in the company.
Change management plan implemented
PASS/ FAIL
Build effective customer relationships
Increase customer contacts
Number of new customer contacts per week
4
Learn and apply communication techniques
Number of feedback sessions
2 per person
LEARNING AND GROWTH (EMPLOYEE) PERSPECTIVE
Promote a culture and working environment that embraces growth and development.
Meet the needs of each of our employees which will more often than not result in employee engagement and employee satisfaction in general.
Ensure that employees are compensated sufficiently which will help with retention.
Today’s competitive environment has, lower manufacturing cost, more productivity in less time, high-quality product, defect-free operation are required to follow to every foundryman. For the improvement of products quality, there are diff-diff quality tools used in various review papers. Here I am going to review these papers and identify the different way of uses of those tools in manufacturing industries to increase the quality of the product. There are so many defects in the manufacturing process and these defects directly affect productivity, profitability and quality level of organization. This study is aimed to review the research work made by several researchers and attempt to get a technical solution for the various defects and to improve the entire process of the manufacturing
Generating ideas is not the issue. Executing on them is. This whitepaper discusses how manufacturers can improve new product development through strategic portfolio management, program execution management, product development, and manufacturing planning and validation. It emphasizes integrating people and processes through capabilities like requirements management, project planning, resource management, and risk management to foster sustainable innovation. Leading companies use product lifecycle management solutions to coordinate development teams and ensure new products meet market needs.
Reducing Inefficency on the Obstetric ServiceRobert Knuppel
This document discusses the need to reduce inefficiencies in obstetric services through implementing process improvement methodologies from business, such as Lean Six Sigma. It notes that obstetrics deals with complex issues and rising costs/risks. Business process improvement approaches can help leadership initiate continuous improvements to patient experience and safety. Some key steps outlined include engaging management, improving communication, conducting structured brainstorming to identify waste/inefficiencies, creating visual maps of current processes, and ensuring reliable data collection to guide improvements. The goal is to standardize processes, reduce variation and waste, and ultimately enhance quality of care while lowering costs.
Product definition starting point for medical device manufacturingKatherine Dalton
The document discusses the importance of product definition as the critical starting point for medical device manufacturing. It states that product definition involves developing a product strategy and plan to define target markets, customers, and competitive strengths. It also involves translating customer needs into a set of product requirements through techniques like Quality Function Deployment. The document emphasizes that properly defining requirements upfront and managing them throughout development is key to minimizing redesign iterations and ensuring medical devices can successfully navigate regulatory processes and certification.
The document discusses various methods for collecting and analyzing data to inform quality improvement projects. It describes process mapping to analyze current processes, brainstorming to generate ideas, surveys to understand stakeholder perspectives, audits to measure performance against standards, and cause and effect diagrams to identify root causes of problems. The goal of using these techniques is to thoroughly diagnose issues to identify opportunities for improving processes and outcomes.
The study of scope and implementation of lean aspectsprj_publication
The document discusses the scope and implementation of lean aspects in the pharmaceutical industry. It begins by noting that pharmaceutical companies face challenges like rising costs and need to deliver quality products quickly within a competitive environment. While other industries have benefited from approaches like Lean and Six Sigma, the pharmaceutical industry has been slow to adopt lean manufacturing.
The study aims to outline the scope for applying lean management principles in the pharmaceutical industry in order to improve quality and efficiency. It conducted surveys at 6 pharmaceutical companies in Hyderabad, India to understand their quality systems and potential for lean implementation. The surveys found awareness of lean was highest through websites and management guides, while business processes showed the lowest awareness. This indicates pharmaceutical firms should look for more opportunities to apply
The study of scope and implementation of lean aspectsprjpublications
The document discusses the scope and implementation of lean aspects in the pharmaceutical industry. It begins with an introduction to lean strategies and their historical use in eliminating waste and improving efficiency. While lean has been successfully adopted in other industries, the pharmaceutical industry has been slow to implement it. The study aims to identify lean management principles that can be applied in the pharmaceutical manufacturing environment to improve quality and productivity while reducing costs. It also discusses conducting surveys of pharmaceutical companies to understand their current quality systems and openness to lean implementation. The goal is to determine how lean principles can enhance processes to achieve very high productivity, short lead times, and exceptional product quality.
How and When to Kill a Program in New Product PlanningAnthony Russell
Presented at the 4th New Product Planning Summit in Boston (Dec 2 -3 , 2019). Presentation covers why weak programs should be cut from pharmaceutical and biotech pipelines, what defines a "weak" program, and describes objective methods to evaluate programs to help prioritize assets.
Project development and implementation for strategic managersBhavi Bhatia
This document outlines tasks and guidelines for developing a new product or service for an organization. It discusses choosing an organization, developing a business case and plan, and identifying costs and resources required. It emphasizes understanding customers, strong product management, identifying the best ideas, proper project management, and support for customization as crucial factors for success. It also discusses evaluating staff training costs, qualitative and quantitative data collection methods, and setting up effective data collection programs.
The document discusses the results of a 2014 survey on the use of data-driven approaches in clinical trials. It finds that while many respondents believe their use of such approaches has advanced in recent years, there is still significant room for improvement. Outsourcing relationships were seen as both promoting and potentially inhibiting their use, by increasing access to data and expertise but also sometimes creating challenges for change management and planning. Overall, the survey highlights opportunities to further apply analytical techniques to optimize clinical development processes and outcomes.
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Integrate RWE into clinical developmentIMSHealthRWES
With greater application of RWE throughout the pharmaceutical
lifecycle, learnings are emerging that offer guidance for
approaches to derive the maximum value. This article captures
the author’s experience at a leading international biotech, with
insights for smoothing RWE assimilation into clinical
development and realizing the benefits it brings.
7 Strategies for Building a Culture of Quality in Manufacturing - Paul A. Arr...marcus evans Network
The medical device industry is facing increased challenges such as cost constraints, decreased spending, and new regulations. Paul Arrendell advises that companies must promote a culture of quality by understanding regulations, validating processes, making quality decisions, and integrating quality throughout the business. He discusses seven strategies for building a quality culture, including design and reliability engineering, robust post-production monitoring, supplier management, quality metrics, incorporating quality into roles and incentives, and learning from other companies' mistakes. Arrendell was speaking at the marcus evans Medical Device Manufacturing and R&D Summits in June 2014.
Similar to Study of the Methods for Decision Making in the Monitoring and Control of Production in the Ecuadorian Pharmaceutical Industries for Project use using Comprehensive Control Panel and Business Architecture (20)
TUNNELING IN HIMALAYAS WITH NATM METHOD: A SPECIAL REFERENCES TO SUNGAL TUNNE...IRJET Journal
1) The document discusses the Sungal Tunnel project in Jammu and Kashmir, India, which is being constructed using the New Austrian Tunneling Method (NATM).
2) NATM involves continuous monitoring during construction to adapt to changing ground conditions, and makes extensive use of shotcrete for temporary tunnel support.
3) The methodology section outlines the systematic geotechnical design process for tunnels according to Austrian guidelines, and describes the various steps of NATM tunnel construction including initial and secondary tunnel support.
STUDY THE EFFECT OF RESPONSE REDUCTION FACTOR ON RC FRAMED STRUCTUREIRJET Journal
This study examines the effect of response reduction factors (R factors) on reinforced concrete (RC) framed structures through nonlinear dynamic analysis. Three RC frame models with varying heights (4, 8, and 12 stories) were analyzed in ETABS software under different R factors ranging from 1 to 5. The results showed that displacement increased as the R factor decreased, indicating less linear behavior for lower R factors. Drift also decreased proportionally with increasing R factors from 1 to 5. Shear forces in the frames decreased with higher R factors. In general, R factors of 3 to 5 produced more satisfactory performance with less displacement and drift. The displacement variations between different building heights were consistent at different R factors. This study evaluated how R factors influence
A COMPARATIVE ANALYSIS OF RCC ELEMENT OF SLAB WITH STARK STEEL (HYSD STEEL) A...IRJET Journal
This study compares the use of Stark Steel and TMT Steel as reinforcement materials in a two-way reinforced concrete slab. Mechanical testing is conducted to determine the tensile strength, yield strength, and other properties of each material. A two-way slab design adhering to codes and standards is executed with both materials. The performance is analyzed in terms of deflection, stability under loads, and displacement. Cost analyses accounting for material, durability, maintenance, and life cycle costs are also conducted. The findings provide insights into the economic and structural implications of each material for reinforcement selection and recommendations on the most suitable material based on the analysis.
Effect of Camber and Angles of Attack on Airfoil CharacteristicsIRJET Journal
This document discusses a study analyzing the effect of camber, position of camber, and angle of attack on the aerodynamic characteristics of airfoils. Sixteen modified asymmetric NACA airfoils were analyzed using computational fluid dynamics (CFD) by varying the camber, camber position, and angle of attack. The results showed the relationship between these parameters and the lift coefficient, drag coefficient, and lift to drag ratio. This provides insight into how changes in airfoil geometry impact aerodynamic performance.
A Review on the Progress and Challenges of Aluminum-Based Metal Matrix Compos...IRJET Journal
This document reviews the progress and challenges of aluminum-based metal matrix composites (MMCs), focusing on their fabrication processes and applications. It discusses how various aluminum MMCs have been developed using reinforcements like borides, carbides, oxides, and nitrides to improve mechanical and wear properties. These composites have gained prominence for their lightweight, high-strength and corrosion resistance properties. The document also examines recent advancements in fabrication techniques for aluminum MMCs and their growing applications in industries such as aerospace and automotive. However, it notes that challenges remain around issues like improper mixing of reinforcements and reducing reinforcement agglomeration.
Dynamic Urban Transit Optimization: A Graph Neural Network Approach for Real-...IRJET Journal
This document discusses research on using graph neural networks (GNNs) for dynamic optimization of public transportation networks in real-time. GNNs represent transit networks as graphs with nodes as stops and edges as connections. The GNN model aims to optimize networks using real-time data on vehicle locations, arrival times, and passenger loads. This helps increase mobility, decrease traffic, and improve efficiency. The system continuously trains and infers to adapt to changing transit conditions, providing decision support tools. While research has focused on performance, more work is needed on security, socio-economic impacts, contextual generalization of models, continuous learning approaches, and effective real-time visualization.
Structural Analysis and Design of Multi-Storey Symmetric and Asymmetric Shape...IRJET Journal
This document summarizes a research project that aims to compare the structural performance of conventional slab and grid slab systems in multi-story buildings using ETABS software. The study will analyze both symmetric and asymmetric building models under various loading conditions. Parameters like deflections, moments, shears, and stresses will be examined to evaluate the structural effectiveness of each slab type. The results will provide insights into the comparative behavior of conventional and grid slabs to help engineers and architects select appropriate slab systems based on building layouts and design requirements.
A Review of “Seismic Response of RC Structures Having Plan and Vertical Irreg...IRJET Journal
This document summarizes and reviews a research paper on the seismic response of reinforced concrete (RC) structures with plan and vertical irregularities, with and without infill walls. It discusses how infill walls can improve or reduce the seismic performance of RC buildings, depending on factors like wall layout, height distribution, connection to the frame, and relative stiffness of walls and frames. The reviewed research paper analyzes the behavior of infill walls, effects of vertical irregularities, and seismic performance of high-rise structures under linear static and dynamic analysis. It studies response characteristics like story drift, deflection and shear. The document also provides literature on similar research investigating the effects of infill walls, soft stories, plan irregularities, and different
This document provides a review of machine learning techniques used in Advanced Driver Assistance Systems (ADAS). It begins with an abstract that summarizes key applications of machine learning in ADAS, including object detection, recognition, and decision-making. The introduction discusses the integration of machine learning in ADAS and how it is transforming vehicle safety. The literature review then examines several research papers on topics like lightweight deep learning models for object detection and lane detection models using image processing. It concludes by discussing challenges and opportunities in the field, such as improving algorithm robustness and adaptability.
Long Term Trend Analysis of Precipitation and Temperature for Asosa district,...IRJET Journal
The document analyzes temperature and precipitation trends in Asosa District, Benishangul Gumuz Region, Ethiopia from 1993 to 2022 based on data from the local meteorological station. The results show:
1) The average maximum and minimum annual temperatures have generally decreased over time, with maximum temperatures decreasing by a factor of -0.0341 and minimum by -0.0152.
2) Mann-Kendall tests found the decreasing temperature trends to be statistically significant for annual maximum temperatures but not for annual minimum temperatures.
3) Annual precipitation in Asosa District showed a statistically significant increasing trend.
The conclusions recommend development planners account for rising summer precipitation and declining temperatures in
P.E.B. Framed Structure Design and Analysis Using STAAD ProIRJET Journal
This document discusses the design and analysis of pre-engineered building (PEB) framed structures using STAAD Pro software. It provides an overview of PEBs, including that they are designed off-site with building trusses and beams produced in a factory. STAAD Pro is identified as a key tool for modeling, analyzing, and designing PEBs to ensure their performance and safety under various load scenarios. The document outlines modeling structural parts in STAAD Pro, evaluating structural reactions, assigning loads, and following international design codes and standards. In summary, STAAD Pro is used to design and analyze PEB framed structures to ensure safety and code compliance.
A Review on Innovative Fiber Integration for Enhanced Reinforcement of Concre...IRJET Journal
This document provides a review of research on innovative fiber integration methods for reinforcing concrete structures. It discusses studies that have explored using carbon fiber reinforced polymer (CFRP) composites with recycled plastic aggregates to develop more sustainable strengthening techniques. It also examines using ultra-high performance fiber reinforced concrete to improve shear strength in beams. Additional topics covered include the dynamic responses of FRP-strengthened beams under static and impact loads, and the performance of preloaded CFRP-strengthened fiber reinforced concrete beams. The review highlights the potential of fiber composites to enable more sustainable and resilient construction practices.
Survey Paper on Cloud-Based Secured Healthcare SystemIRJET Journal
This document summarizes a survey on securing patient healthcare data in cloud-based systems. It discusses using technologies like facial recognition, smart cards, and cloud computing combined with strong encryption to securely store patient data. The survey found that healthcare professionals believe digitizing patient records and storing them in a centralized cloud system would improve access during emergencies and enable more efficient care compared to paper-based systems. However, ensuring privacy and security of patient data is paramount as healthcare incorporates these digital technologies.
Review on studies and research on widening of existing concrete bridgesIRJET Journal
This document summarizes several studies that have been conducted on widening existing concrete bridges. It describes a study from China that examined load distribution factors for a bridge widened with composite steel-concrete girders. It also outlines challenges and solutions for widening a bridge in the UAE, including replacing bearings and stitching the new and existing structures. Additionally, it discusses two bridge widening projects in New Zealand that involved adding precast beams and stitching to connect structures. Finally, safety measures and challenges for strengthening a historic bridge in Switzerland under live traffic are presented.
React based fullstack edtech web applicationIRJET Journal
The document describes the architecture of an educational technology web application built using the MERN stack. It discusses the frontend developed with ReactJS, backend with NodeJS and ExpressJS, and MongoDB database. The frontend provides dynamic user interfaces, while the backend offers APIs for authentication, course management, and other functions. MongoDB enables flexible data storage. The architecture aims to provide a scalable, responsive platform for online learning.
A Comprehensive Review of Integrating IoT and Blockchain Technologies in the ...IRJET Journal
This paper proposes integrating Internet of Things (IoT) and blockchain technologies to help implement objectives of India's National Education Policy (NEP) in the education sector. The paper discusses how blockchain could be used for secure student data management, credential verification, and decentralized learning platforms. IoT devices could create smart classrooms, automate attendance tracking, and enable real-time monitoring. Blockchain would ensure integrity of exam processes and resource allocation, while smart contracts automate agreements. The paper argues this integration has potential to revolutionize education by making it more secure, transparent and efficient, in alignment with NEP goals. However, challenges like infrastructure needs, data privacy, and collaborative efforts are also discussed.
A REVIEW ON THE PERFORMANCE OF COCONUT FIBRE REINFORCED CONCRETE.IRJET Journal
This document provides a review of research on the performance of coconut fibre reinforced concrete. It summarizes several studies that tested different volume fractions and lengths of coconut fibres in concrete mixtures with varying compressive strengths. The studies found that coconut fibre improved properties like tensile strength, toughness, crack resistance, and spalling resistance compared to plain concrete. Volume fractions of 2-5% and fibre lengths of 20-50mm produced the best results. The document concludes that using a 4-5% volume fraction of coconut fibres 30-40mm in length with M30-M60 grade concrete would provide benefits based on previous research.
Optimizing Business Management Process Workflows: The Dynamic Influence of Mi...IRJET Journal
The document discusses optimizing business management processes through automation using Microsoft Power Automate and artificial intelligence. It provides an overview of Power Automate's key components and features for automating workflows across various apps and services. The document then presents several scenarios applying automation solutions to common business processes like data entry, monitoring, HR, finance, customer support, and more. It estimates the potential time and cost savings from implementing automation for each scenario. Finally, the conclusion emphasizes the transformative impact of AI and automation tools on business processes and the need for ongoing optimization.
Multistoried and Multi Bay Steel Building Frame by using Seismic DesignIRJET Journal
The document describes the seismic design of a G+5 steel building frame located in Roorkee, India according to Indian codes IS 1893-2002 and IS 800. The frame was analyzed using the equivalent static load method and response spectrum method, and its response in terms of displacements and shear forces were compared. Based on the analysis, the frame was designed as a seismic-resistant steel structure according to IS 800:2007. The software STAAD Pro was used for the analysis and design.
Cost Optimization of Construction Using Plastic Waste as a Sustainable Constr...IRJET Journal
This research paper explores using plastic waste as a sustainable and cost-effective construction material. The study focuses on manufacturing pavers and bricks using recycled plastic and partially replacing concrete with plastic alternatives. Initial results found that pavers and bricks made from recycled plastic demonstrate comparable strength and durability to traditional materials while providing environmental and cost benefits. Additionally, preliminary research indicates incorporating plastic waste as a partial concrete replacement significantly reduces construction costs without compromising structural integrity. The outcomes suggest adopting plastic waste in construction can address plastic pollution while optimizing costs, promoting more sustainable building practices.
Embedded machine learning-based road conditions and driving behavior monitoringIJECEIAES
Car accident rates have increased in recent years, resulting in losses in human lives, properties, and other financial costs. An embedded machine learning-based system is developed to address this critical issue. The system can monitor road conditions, detect driving patterns, and identify aggressive driving behaviors. The system is based on neural networks trained on a comprehensive dataset of driving events, driving styles, and road conditions. The system effectively detects potential risks and helps mitigate the frequency and impact of accidents. The primary goal is to ensure the safety of drivers and vehicles. Collecting data involved gathering information on three key road events: normal street and normal drive, speed bumps, circular yellow speed bumps, and three aggressive driving actions: sudden start, sudden stop, and sudden entry. The gathered data is processed and analyzed using a machine learning system designed for limited power and memory devices. The developed system resulted in 91.9% accuracy, 93.6% precision, and 92% recall. The achieved inference time on an Arduino Nano 33 BLE Sense with a 32-bit CPU running at 64 MHz is 34 ms and requires 2.6 kB peak RAM and 139.9 kB program flash memory, making it suitable for resource-constrained embedded systems.
Presentation of IEEE Slovenia CIS (Computational Intelligence Society) Chapte...University of Maribor
Slides from talk presenting:
Aleš Zamuda: Presentation of IEEE Slovenia CIS (Computational Intelligence Society) Chapter and Networking.
Presentation at IcETRAN 2024 session:
"Inter-Society Networking Panel GRSS/MTT-S/CIS
Panel Session: Promoting Connection and Cooperation"
IEEE Slovenia GRSS
IEEE Serbia and Montenegro MTT-S
IEEE Slovenia CIS
11TH INTERNATIONAL CONFERENCE ON ELECTRICAL, ELECTRONIC AND COMPUTING ENGINEERING
3-6 June 2024, Niš, Serbia
A review on techniques and modelling methodologies used for checking electrom...nooriasukmaningtyas
The proper function of the integrated circuit (IC) in an inhibiting electromagnetic environment has always been a serious concern throughout the decades of revolution in the world of electronics, from disjunct devices to today’s integrated circuit technology, where billions of transistors are combined on a single chip. The automotive industry and smart vehicles in particular, are confronting design issues such as being prone to electromagnetic interference (EMI). Electronic control devices calculate incorrect outputs because of EMI and sensors give misleading values which can prove fatal in case of automotives. In this paper, the authors have non exhaustively tried to review research work concerned with the investigation of EMI in ICs and prediction of this EMI using various modelling methodologies and measurement setups.
Understanding Inductive Bias in Machine LearningSUTEJAS
This presentation explores the concept of inductive bias in machine learning. It explains how algorithms come with built-in assumptions and preferences that guide the learning process. You'll learn about the different types of inductive bias and how they can impact the performance and generalizability of machine learning models.
The presentation also covers the positive and negative aspects of inductive bias, along with strategies for mitigating potential drawbacks. We'll explore examples of how bias manifests in algorithms like neural networks and decision trees.
By understanding inductive bias, you can gain valuable insights into how machine learning models work and make informed decisions when building and deploying them.
International Conference on NLP, Artificial Intelligence, Machine Learning an...gerogepatton
International Conference on NLP, Artificial Intelligence, Machine Learning and Applications (NLAIM 2024) offers a premier global platform for exchanging insights and findings in the theory, methodology, and applications of NLP, Artificial Intelligence, Machine Learning, and their applications. The conference seeks substantial contributions across all key domains of NLP, Artificial Intelligence, Machine Learning, and their practical applications, aiming to foster both theoretical advancements and real-world implementations. With a focus on facilitating collaboration between researchers and practitioners from academia and industry, the conference serves as a nexus for sharing the latest developments in the field.
CHINA’S GEO-ECONOMIC OUTREACH IN CENTRAL ASIAN COUNTRIES AND FUTURE PROSPECTjpsjournal1
The rivalry between prominent international actors for dominance over Central Asia's hydrocarbon
reserves and the ancient silk trade route, along with China's diplomatic endeavours in the area, has been
referred to as the "New Great Game." This research centres on the power struggle, considering
geopolitical, geostrategic, and geoeconomic variables. Topics including trade, political hegemony, oil
politics, and conventional and nontraditional security are all explored and explained by the researcher.
Using Mackinder's Heartland, Spykman Rimland, and Hegemonic Stability theories, examines China's role
in Central Asia. This study adheres to the empirical epistemological method and has taken care of
objectivity. This study analyze primary and secondary research documents critically to elaborate role of
china’s geo economic outreach in central Asian countries and its future prospect. China is thriving in trade,
pipeline politics, and winning states, according to this study, thanks to important instruments like the
Shanghai Cooperation Organisation and the Belt and Road Economic Initiative. According to this study,
China is seeing significant success in commerce, pipeline politics, and gaining influence on other
governments. This success may be attributed to the effective utilisation of key tools such as the Shanghai
Cooperation Organisation and the Belt and Road Economic Initiative.
CHINA’S GEO-ECONOMIC OUTREACH IN CENTRAL ASIAN COUNTRIES AND FUTURE PROSPECT
Study of the Methods for Decision Making in the Monitoring and Control of Production in the Ecuadorian Pharmaceutical Industries for Project use using Comprehensive Control Panel and Business Architecture