We have for you a well disciplined team of competent and qualified Auditors, Lead Auditors and Experts having rich and long experience in the second party and thirty party auditing against requirements of ISO 9001, ISO 14001 ISO 13485, Medical Device Directive 93/42/EEC, US FDA cGMP as set forth in QSR which is part 820 of 21 CFR.

In addition we have at your disposal Auditors, Lead Auditors and Experts for ISO 22000, OHSAS 18001, SA 8000.

For further information please call us or advise through email.