Does your QC lab do GMP and non-GMP activities? 2018 is a webinar that covers topics such as:
- CFR guidance for GLP practices and method and procedure development
- CFR guidance for GMP testing of pharmaceutical products
- The transition from a procedure in development to one used routinely
- Product testing and regulatory requirements
- Establishing boundaries
- The use of test plans
Does your QC lab do GMP and non-GMP activities? 2018 is intended for:
- QC technical transfer groups
- QC functions in general
- Commercial testing facilities
- QC validation groups
- QA reviewers who are responsible for both GMP and GLP documentation practices
- Product development
