We do what we can do best
Our quality requirements and the Good Manufacturing Practice (GMP) guidelines are the focus of our activities.
This is additionally ensured by a sophisticated quality management system that integrates all required aspects.
In terms of “quality assurance”, we see ourselves as the link facilitating constructive collaboration between different LPH departments, with the goal of continuously ensuring the quality of our products and user safety for our patients.
Our experienced, qualified staff are responsible for compliance with GMP guidelines and relevant pharmaceutical law-related provisions during the production, inspection and approval of medical products.
We have qualified rooms and systems, as well as validated cleaning processes for pharmaceutical contract manufacturing.
Our quality assurance includes:
- User safety of products
- Work processes based on certified instructions
- Complete documentation
- Pharmaceutically qualified rooms and equipment
- Qualified and trained expert staff
- Validated production processes
- Controlled change processes