»  Our Commitment
Our commitment to human society encourages us to establish and maintain a top quality system to achieve our top desired goals in the healthcare world. Our Quality activities start from the time that raw materials are received and continue until the final product is used by the end users in order to find required results.

Quality Assurance department of CinnaGen has the responsibility for Documentation, Validation, Inspection and Auditing, batch release, and post marketing surveillance and carries out the duties according to the latest WHO and ICH Guidelines. In 2000, CinnaGen with the full support of its personnel was granted ISO 9000 certificate for Quality management from TUV Rheinland.

CinnaGen’s QC laboratories are equipped with all necessary reagents and equipment to perform complete QC tests for biological products and enjoy the collaboration with the best international experts in this field. For quality of our products, no limit has been set forth. We constantly make attempts to be up- to date with various regulations and guidelines according to our customers’ demand.

We try to be the best GMP implementation company among pharmaceutical manufacturers in the whole region.