GMP - Compliance for Voltaren

Date: 21.06.2023
Time: 09:00 - 17:00
Location: Online

The workshop intensively simulates daily business of all employees within a pharmaceutical company that contribute to a finished drug product: here Voltaren. EU GMP guideline consists of nine chapters demanding individual requirements which must be fulfilled by different departments in order to be authorized to produce and sell this drug. It is much more than production and testing. GMP requires a solid environment that needs tob e established.

Interactive Part: We will split into 9 groups elaborating all GMP requirements for Voltaren production including raw materials supply, manufacturing, quality control, quality assurance. In the end our quality team will perform an internal audit to control completeness.