GxP commonly refers to the standard quality management systems in pharmaceutical, chemical, biotechnology, food, and medical device industries. This three-day training offers a comprehensive overview of internationally required quality assurance systems in regulated research and development (R&D) focusing on Good Laboratory Practice (GLP), Good Clinical Practice (GCP), and Good Manufacturing Practice (GMP). Participants will learn about study processes, data management, regulatory requirements, documentation and data integrity practices, as well as audits and inspections. Practical examples provide valuable insights into research, development and production.

The course is particularly suitable for graduates, doctoral students and postdocs from the fields of medicine, biology, chemistry and life sciences, as well as for anyone seeking insight into quality assurance in pharmaceutical and biotech companies.

Duration: 3 days