PURSUIT OF CLINICAL QUALITY

As a part of our efforts to offer the best solutions, we are committed to adhere to all the local and international standards. This is to fulfil and assure you, our clients, our unwavering commitment to quality, efficacy and efficiency, one such proof is our commitment that we are registered with the Saudi Food and Drug Authority [SFDA] and we strive to comply with all their rules and regulations.

We have obtained from the SFDA the following registrations and certificates:

1 - MDNR
2 - MDELS
3 - MDMA

Collaborating Overseas Clinical Laboratory
The ImuPro test uses the ELISA Laboratory Test method - the standard procedure recognized in medical laboratories. Our collaborating laboratory in Germany is modern and well equipped.

INTERNATIONAL ACCREDITATION

The ImuPro300 Test follows Annex 111 of the EC Directive 98/79 EC, which is an internationally recognized Quality Management System accredited under the Medical Device Directive EN ISO 9001. The Test is ISO-9999 certified with CE approval in addition to the Therapeutic Goods Association (TGA) standard of approval.