GMP – Good Manufacturing Practice
Half day course – Online
This course will show documentation requirements under GMP regulations for the Medical Device and In Vitro Diagnostic industry.
Documentation in this type of industry is expected to have a high level of traceability in the complete manufacturing process (for methods, facilities, and controls used in manufacturing, processing, and packing of a product). Purpose of following GMP is to, with a risk-based approach, minimize or eliminate instances of contamination, mix-ups, and errors. The traceability simplifies evaluations and improvements of the product and process, when needed.
For details on registration and price for member companies to Swedish Labtech go to Swedish Labtech
- When: to
- Where: Online
- Organizer: Swedish Labtech in co-operation with QAdvis AB
- Language: Swedish
- Price: 5500 VAT not included
Please register no later than Thursday 29 September 2022