ComplianceOnline, Online Event
Why Should You Attend: Analytical methods play a key role in assuring that drug substances and drug products conform to their specifications. Demonstrating that these methods consistently perform appropriately for their intended purpose can be both challenging and resource intensive. By using a pro-active, quality-by-design (QbD) approach, it is possible to design better methods, understand the strengths, weaknesses and capabilities of those method and to perform validation exercises in a scientifically rational way that will maximize success and minimize overall resource consumption. This is especially true for the method transfer process, where many examples of tremendous complication can be cited due to inadequacy in method design and development, and due to inappropriate design of method transfer protocols.
This course is designed to provide participants with a lifecycle approach to developing and validating analytical methods. By using a lifecycle approach, methods are more likely to meet their intended purpose, and scientists are more likely to have success during validation and transfer exercises. This approach will be linked with current compendial requirements.
After attending this course, you’ll understand the interconnectedness of these phases in the lifecycle of an analytical method and be prepared to plan for success. By appropriate planning, you can avoid the pitfalls of methods which fail validation protocols, of ‘validated’ methods which do not perform adequately in routing use and of transfers to other sites which fail, resulting in production delays, regulatory scrutiny, frustration and waste of valuable resources.
Areas Covered in the seminar:
- Understand the lifecycle approach to method development and validation.
- Identify an Analytical Target Profile for Methods Being Developed.
- Use an IQ/OQ/PQ Approach to Method Qualification.
- Develop Appropriate Protocols for Method Transfer.
- Comply with Compendial Requirements with Greater Success and Fewer Resources.
Who Will Benefit:
This webinar will provide valuable assistance to all Biotech & Pharmaceutical companies/ manufacturing sites. Those that would benefit most would be:
- Chemists (Research, Quality Control, CRO) involved with analytical method development, validation or transfer and their managers
- Regulatory affairs/CMC personnel responsible for documenting analytical methods and their acceptability
- Laboratory managers and staff
- QA/QCU managers and personnel
- Training department
- Documentation department
NOTE: Use This Promocode ( 117660 ) To Get 10% Discount.
Gregory Martin, is the founder and President of Complectors Consulting LLC, which provides consulting and training in the area of Pharmaceutical Analytical Chemistry. Greg is Vice Chair of the USP General Chapters Expert Committee, and has over 29 years experience in the pharmaceutical industry, including ten years as Director of Pharmaceutical Analytical Chemistry in Merck Research Laboratories. Greg's interests include impurities and residual solvents, dissolution, analytical instrument qualification and other topics related to laboratory GMP compliance.