QM systems and GMP consulting
Diapharm assists clients by establishing new quality management systems for medicinal products and medical devices and by monitoring existing ones. We help you prepare for GMP audits and ISO audits, to adapt to changing requirements, to check manufacturing processes (compliance check) and much more…
- QM system setup in accordance with GMP for medicinal products
- QM system setup in accordance with ISO 13485 for medical devices
- Update existing quality management systems
- GMP consulting
- Carrying out self inspections
- Assistance with inspections performed by regulatory authorities
Diapharm ensures that you have a pharmaceutical quality management system that fits your needs. Our consultants develop QM manuals and standard operating procedures (SOPs) in the way that standardised QM processes reflect the individual workflows at your company. This, however, is not a contradiction in terms; it is appropriate – and efficient.
Did you know: In addition to consulting on GMP issues, Diapharm assumes duties and responsibilities in your QM system, for example acting as the quality management officer.
