GMP Compliance for Quality Control and Contract Laboratories 2017 covers topics such as:
- The company’s quality plan or laboratory compliance master plan
- Regulatory background and GMP requirements for quality control and contract laboratories
- How to develop inspection ready documentation
- The difference between GMP and non-GMP laboratories
- How to avoid and/or respond to the FDA inspectional observations and warning letters
GMP Compliance for Quality Control and Contract Laboratories 2017 brings together personnel in FDA regulated laboratories, including:
- QA managers and personnel
- Analysts and lab managers
- Regulatory affairs
- Validation specialists
- Human resources (HR) managers and staff
- IT professionals
- Documentation department
- Training departments
- Consultants& teachers
