Good Manufacturing Practice course
About the course:
Pharmaceutical Good Manufacturing Practice (GMP) principles are set through the world as international standards for quality pharmaceutical production. GMP standards assure that pharmaceutical manufacturing is well managed and aimed on production of quality pharmaceutical products. The course is based on World Health Organisation’s Guidelines for Pharmaceutical Good Manufacturing Practices and EU Directives on Good Manufacturing Practices (The Rules Governing Medicinal Products in the European Union, Volume 4, EU Guidelines to Good Manufacturing Practice Medicinal Products for Human and Veterinary Use). The course is designed to give pharmaceutical production personnel up-to date information about international requirements to pharmaceutical production.
Who should attend:
The course is designed for pharmaceutical production, quality control and assurance personnel.
Certificates of completion are given to course participants upon successful graduation.
The course covers all essential elements of GMP and consists of the following parts:
- Quality Management,
- Premises and Equipment,
- Production operations,
- Quality Control operations,
- Inspection and Audit.
The course comes with a comprehensive manual, which proves to be an excellent handout and source of reference after the course.