We continually strive to meet and maintain the highest standards in the products and services we provide.
Our commitment to quality is exemplified by our:
- ISO 9001 Quality Management System certification
- Authorization for Good distribution practice for active pharmaceutical ingredients (API)
- Registration as a Medical Device Distributor
- Collaboration with reliable providers
ISO 9001 Quality management system
The ISO 9001:2008-certified Quality management system ensures we deliver quality services and products to our clients and partners. At the same time, the system challenges us to continually improve our processes and approaches in order to deliver the best possible results. The ISO 9001 certification comes as a recognition of long term commitment to consistency, to continual improvement and to customer satisfaction.
Good distribution practice for active substances (GDP)
Trasis is certified as meeting the standards of Good distribution practice for active substances used as starting materials in medicinal products for human use, in accordance with Guidelines of 19 March 2015 on principles of Good Distribution Practice of active substances for medicinal products for human (2015/C 95/01). This covers more specifically the receipt, storage, delivery to customers and returns of substances, as well as complaints and recalls.
Our certification acknowledges that the chemicals distributed by Trasis are obtained from a licensed supply chain, are consistently stored, transported and handled. This certification allows our customers to justify that GMP chemical products will suffer no alteration while handled by Trasis.
Medical device distributor
Trasis is registered at the Belgian Federal Agency for Medecines and Health Products (FAMHP) as a distributor of medical devices, in accordance with the Royal Decree of 18 March 1999 on medical devices