Does your QC lab do GMP and non-GMP activities? 2018

Topics

• 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

Who should Attend

• 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