Lifecycle Management 2021 - Lifecycle Management of Analytical Methods and Procedures - according to new FDA and USP guidelines Training
Topics/Call fo Papers
Faculty Response The answer is yes because they have expertise necessary to ensure that the system they have designed, provided and delivered to you is operating in accordance with user specifications.
Results of analytical methods are used as the basis for important decisions during development and manufacturing of pharmaceutical products. All regulatory agencies expect
The importance of analytical procedures
ICH Q12
Introduction to lifecycle management of analytical methods
Speaker:
Ms. Thomas has over two decades of cGMP hands-on industry experience in both pharmaceutical and medical device manufacturing operations.
Results of analytical methods are used as the basis for important decisions during development and manufacturing of pharmaceutical products. All regulatory agencies expect
The importance of analytical procedures
ICH Q12
Introduction to lifecycle management of analytical methods
Speaker:
Ms. Thomas has over two decades of cGMP hands-on industry experience in both pharmaceutical and medical device manufacturing operations.
Other CFPs
- Best Practices for Auditing a Vendor of Computer Systems Regulated by FDA
- Risk Based Verification and/or Validation to meet US FDA CGMP and ISO 13485 Requirements
- Privacy Issues in the Workplace
- Workplace Violence and Active Threat Response: Preparation and Readiness Topics
- Performance Appraisals That Motivate and Limit Legal Liability
Last modified: 2020-12-30 23:29:43