ISO certified
As product innovation is the core focus of the company, R&D and Quality Management are at the foundation of BioClin. The company is ISO 13485 certified (annex II) which is the strictest quality standard for Medical Device handling. Operational affairs are outsourced in a contracted network of well recognized specialized laboratories and contract-manufacturing locations in The Netherlands and in various other EU countries. All this in order to maintain the highest pharmaceutical standard related to safety and clinical evaluation.
BioClin is as a legal manufacturer responsible for the quality of its products and for that reason the contract manufacturing production sites have GMP or ISO certification.

