Bringing Existing Factories Into Compliance with EU Good Manufacturing Practice (EU cGMP)
In order to bring Chinese partners into compliance, Stravencon fields a team headed by a Qualified Person (QP), required for product release in Europe. The team includes EU pharmacists, pharmaceutical engineers, medical doctors and experienced pharmaceutical executives.
This team implements a full audit and follows up with specific recommendations for the improvements, reconstruction and re-training of staff required to gain approval by an EU regulatory authority.
