CGMP: A Complete Guide
Course Overview This comprehensive course provides a thorough understanding of Current Good Manufacturing Practices (CGMP) for the pharmaceutical, biotechnology, and medical device industries. Participants will gain a deep understanding of the regulations, guidelines, and best practices for ensuring the quality, safety, and efficacy of products.
Course Objectives - Understand the history and evolution of CGMP
- Learn the key principles and guidelines of CGMP
- Understand the role of CGMP in ensuring product quality, safety, and efficacy
- Apply CGMP principles to real-world scenarios
- Develop a comprehensive understanding of CGMP regulations and guidelines
Course Outline Module 1: Introduction to CGMP
- History and evolution of CGMP
- Key principles and guidelines of CGMP
- Overview of CGMP regulations and guidelines
- Importance of CGMP in ensuring product quality, safety, and efficacy
Module 2: CGMP Regulations and Guidelines
- Overview of FDA regulations and guidelines
- Understanding 21 CFR Part 211
- Understanding 21 CFR Part 820
- EU GMP regulations and guidelines
- ICH guidelines
Module 3: Quality Management Systems
- Overview of quality management systems
- Understanding ISO 9001
- Understanding ISO 13485
- Quality policy and objectives
- Quality planning and control
Module 4: Facility Design and Construction
- Overview of facility design and construction
- Understanding cleanroom design and construction
- Understanding HVAC systems
- Understanding water systems
- Waste management and disposal
Module 5: Equipment and Instrumentation
- Overview of equipment and instrumentation
- Understanding equipment qualification and validation
- Understanding calibration and maintenance
- Understanding instrumentation and control systems
- Computerized systems and software validation
Module 6: Materials Management
- Overview of materials management
- Understanding material sourcing and procurement
- Understanding material storage and handling
- Understanding material testing and inspection
- Supplier qualification and management
Module 7: Production and Process Controls
- Overview of production and process controls
- Understanding batch processing and control
- Understanding continuous processing and control
- Understanding process validation and verification
- Understanding cleaning and sanitization
Module 8: Packaging and Labeling
- Overview of packaging and labeling
- Understanding packaging design and development
- Understanding packaging materials and components
- Understanding labeling and labeling controls
- Understanding packaging and labeling regulations and guidelines
Module 9: Laboratory Controls
- Overview of laboratory controls
- Understanding laboratory design and layout
- Understanding laboratory equipment and instrumentation
- Understanding laboratory testing and inspection
- Understanding laboratory data management and reporting
Module 10: Documentation and Record Keeping
- Overview of documentation and record keeping
- Understanding document control and management
- Understanding record keeping and retention
- Understanding electronic records and electronic signatures
- Understanding documentation and record keeping regulations and guidelines
Module 11: Training and Competence
- Overview of training and competence
- Understanding training needs assessment and planning
- Understanding training delivery and evaluation
- Understanding competence assessment and evaluation
- Understanding training and competence regulations and guidelines
Module 12: Audits and Inspections
- Overview of audits and inspections
- Understanding audit and inspection types and purposes
- Understanding audit and inspection preparation and planning
- Understanding audit and inspection execution and reporting
- Understanding audit and inspection follow-up and closure
Module 13: Corrective and Preventive Action
- Overview of corrective and preventive action
- Understanding corrective action and preventive action concepts
- Understanding corrective action and preventive action procedures
- Understanding corrective action and preventive action implementation and evaluation
- Understanding corrective action and preventive action regulations and guidelines
Module 14: Continuous Improvement
- Overview of continuous improvement
- Understanding continuous improvement concepts and principles
- Understanding continuous improvement tools and techniques
- Understanding continuous improvement implementation and evaluation
- Understanding continuous improvement regulations and guidelines
Certificate of Completion Upon completion of this course, participants will receive a Certificate of Completion issued by The Art of Service.
Course Features - Interactive and engaging content
- Comprehensive and up-to-date information
- Personalized learning experience
- Practical and real-world applications
- High-quality content and expert instructors
- Certification upon completion
- Flexible learning schedule
- User-friendly and mobile-accessible platform
- Community-driven and interactive discussions
- Actionable insights and hands-on projects
- Bite-sized lessons and lifetime access
- Gamification and progress tracking
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- Understand the history and evolution of CGMP
- Learn the key principles and guidelines of CGMP
- Understand the role of CGMP in ensuring product quality, safety, and efficacy
- Apply CGMP principles to real-world scenarios
- Develop a comprehensive understanding of CGMP regulations and guidelines