GMP Compliance for Pharmaceutical Quality Control Laboratories 2015 is a seminar that covers topics such as:
- Dealing with external laboratories
- Different types of QC laboratories, including contract laboratories
- Animal testing and GLP laboratories
- The instruments and laboratory are qualified? Aren`t they?
- The Microbiology Laboratory
- The GMP regulations
- Test Method Validations
- Out-of-Specification (OOS) test results
- Dealing with multiple outcomes from different sources
- Statistical problems with testing
GMP Compliance for Pharmaceutical Quality Control Laboratories 2015 is intended for:
- Managers
- Directors
- Manufacturing
- Supervisors, and lead workers in Product and Process Development
- Quality Assurance and Quality Control
- Regulatory Affairs
- Manufacturing, or testing of medicinal products will benefit from knowing the procedures and applications applicable to the quality control laboratory
- Quality Control workers who will be participating in operations or the supervision of the development