Achira is now recommended for ISO 13485-2016 by TUV

Achira a leading medical device research company has now been successfully recommended for ISO 13485 Certification by TUV.

The entire journey started with gap analysis, preparation of documentation, preparation of the design file, review of the management system, internal audits, stage 1 and stage 2 audit by TUV.

Risk assessment were carried out based on the special ISO standard for carrying out risk assessment for medical devices.

Wish to know more about ISO 13485-2016 Consulting for medical devices, ISO 13485 Certification for medical device research center, production center, service drop an email to [email protected] or call on 9845313910, 9741501910.