3-Hour Virtual Seminar on Fundamentals of GMPs – Good Manufacturing Practices
Strengthen GMPs Today to Avoid Costly Lawsuits, Lost Licensure, and Damaged Reputations!
Instructor :
Charles H. Paul
Webinar ID:
4312
Date: 21 February 23, TUE
Start Time: 10 am PT
Duration: 3 Hrs.
What you will learn
- What are the regulations governing Good Manufacturing Practices?
- Quality Management, Personnel, Premises and equipment
- Documentation, Production, Quality Assurance
- Materials management, Production and in-process controls
- What are the regulations governing Good Manufacturing Practices?
- Quality Management, Personnel, Premises and equipment
- Documentation, Production, Quality Assurance
- Materials management, Production and in-process controls
- Packaging and labeling, Storage and distribution
- Laboratory controls, Validation, Change control
- Rejection and re-use of material, Complaints and recalls, Supplier controls
Course Description
What are Good Manufacturing Practices?
They are a set of practices that are required to comply with regulations and industry standards that insure that your products are effective as claimed and are pure and defect free.
GMPs minimize the risks associated with processing and manufacturing products. Every country to include the US with the FDA has their own set of governing GMP regulations. Some of these regulations are harmonized with others while some are not.
These regulations are not guidelines…they have the weight of law. They essentially dictate how work and the workers executing that work must conduct their work activities. GMPs touch upon virtually every aspect of work life and the processes that are performed as integral components of that work.
GMPs govern the methods used in, and the facilities and controls used for:
- The design, manufacture
- Packaging, labeling,
- Storage, installation, and servicing of all finished products intended for human use.
The purpose of these regulation? It is very simple – to ensure that medical/medicinal are safe and effective.
Achieving this safety and effectiveness requirement however is not so simple. It is achieved by implementing what is known as a Quality System consisting of many regulatory requirements as specified in the governing regulations that must be:
- Documented in the form of Standard Operating Procedures and Work Instructions
- Integrated into the fabric of how the business executes the activities required to place a medical/medicinal product into the marketplace
- Be managed on a daily basis to ensure the organization’s compliance to the tenants of the regulation
- Be provable when externally audited to verify its effectiveness and compliance with the regulation
Charles H. Paul will guide you on how exactly you can achieve it successfully.
Enroll Now!
What are Good Manufacturing Practices?
They are a set of practices that are required to comply with regulations and industry standards that insure that your products are effective as claimed and are pure and defect free.
GMPs minimize the risks associated with processing and manufacturing products. Every country to include the US with the FDA has their own set of governing GMP regulations. Some of these regulations are harmonized with others while some are not.
These regulations are not guidelines…they have the weight of law. They essentially dictate how work and the workers executing that work must conduct their work activities. GMPs touch upon virtually every aspect of work life and the processes that are performed as integral components of that work.
GMPs govern the methods used in, and the facilities and controls used for:
- The design, manufacture
- Packaging, labeling,
- Storage, installation, and servicing of all finished products intended for human use.
The purpose of these regulation? It is very simple – to ensure that medical/medicinal are safe and effective.
Achieving this safety and effectiveness requirement however is not so simple. It is achieved by implementing what is known as a Quality System consisting of many regulatory requirements as specified in the governing regulations that must be:
- Documented in the form of Standard Operating Procedures and Work Instructions
- Integrated into the fabric of how the business executes the activities required to place a medical/medicinal product into the marketplace
- Be managed on a daily basis to ensure the organization’s compliance to the tenants of the regulation
- Be provable when externally audited to verify its effectiveness and compliance with the regulation
Charles H. Paul will guide you on how exactly you can achieve it successfully.
Enroll Now!
Why you should attend
Overlooking the importance of GMP for regulated medicinal products is a big mistake!
Not following GMP can result in serious health risks if the manufactured product is put in the hands of consumers. An unsafe product that reaches the market can result in costly lawsuits, lost licensure, and damaged reputations!
If you work within regulated medical product industries, almost everything that you do every day is somehow touched by this regulation.
Ignorance of the sections of this regulation is no excuse for non-compliance. It takes a complete thorough understanding of the regulation to ensure your compliance to it.
This webinar will provide that level of understanding and some basic guidance to assure compliance.
Join Now!
Overlooking the importance of GMP for regulated medicinal products is a big mistake!
Not following GMP can result in serious health risks if the manufactured product is put in the hands of consumers. An unsafe product that reaches the market can result in costly lawsuits, lost licensure, and damaged reputations!
If you work within regulated medical product industries, almost everything that you do every day is somehow touched by this regulation.
Ignorance of the sections of this regulation is no excuse for non-compliance. It takes a complete thorough understanding of the regulation to ensure your compliance to it.
This webinar will provide that level of understanding and some basic guidance to assure compliance.
Join Now!
Areas Covered
- What are the regulations governing Good Manufacturing Practices?
- Quality Management
- Personnel
- Premises and equipment
- Documentation
- Production
- Quality Assurance
- Materials management
- Production and in-process controls
- Packaging and labeling
- Storage and distribution
- Laboratory controls
- Validation
- Change control
- Rejection and re-use of material
- Complaints and recalls
- Supplier controls
- What are the regulations governing Good Manufacturing Practices?
- Quality Management
- Personnel
- Premises and equipment
- Documentation
- Production
- Quality Assurance
- Materials management
- Production and in-process controls
- Packaging and labeling
- Storage and distribution
- Laboratory controls
- Validation
- Change control
- Rejection and re-use of material
- Complaints and recalls
- Supplier controls
Who is this course for
Anyone involved in the production of GMP regulated medicinal products – pharmaceuticals, medical devices, and biologics!
NOTE: This webinar applies to all worker levels – Associates, Managers, Directors, Vice- Presidents.
Functions:
- Research & Development
- Technical Services
- Manufacturing
- Compliance and Regulatory
- Quality Assurance and Quality Control
- Logistics/Supply chain
- Service and Maintenance
- Marketing
Anyone involved in the production of GMP regulated medicinal products – pharmaceuticals, medical devices, and biologics!
NOTE: This webinar applies to all worker levels – Associates, Managers, Directors, Vice- Presidents.
Functions:
- Research & Development
- Technical Services
- Manufacturing
- Compliance and Regulatory
- Quality Assurance and Quality Control
- Logistics/Supply chain
- Service and Maintenance
- Marketing
Instructor Profile
Charles H. Paul is the President of C. H. Paul Consulting, Inc. – a regulatory, training, and technical documentation consulting firm. Charles has been a regulatory consultant to the life sciences industry for over 20 years and has published numerous white papers on the subject. The firm works with both domestic and international clients designing solutions for complex human performance and compliance-related problems.
