GMP Compliance for Quality Control and Contract Laboratories: 2-day In-person Seminar

Quality control and related contract laboratories are considered at high risk because after testing and approval, drug products and Active Pharmaceutical Ingredients (APIs) are released to the market without further check. That's the reason why the FDA and other agencies put highest emphasis on inspections of QC laboratories. Even though cGMP regulations have been in place since long time, the large number of QC related 483's and warning letters demonstrate that companies have problems with implementation.

• Learn about the regulatory background and GMP requirements for quality control and contract laboratories.
• Understand and be able to explain your company’s quality plan or laboratory compliance master plan.
• Understand the difference between GMP and non-GMP laboratories.
• Learn how to develop inspection ready documentation.
• Be able to train others in your organization on GMP requirements.

This seminar will be beneficial to the following personnel in FDA regulated laboratories:

• Analysts and lab managers
• QA managers and personnel
• Validation specialists
• Regulatory affairs
• IT professionals
• Human resources (HR) managers and staff

Use coupon code 232082 and get 10% off on registration.