admin, Author at Registitute

27 Aug 23

Announcing Our Expansion: Partnering with Leading Clinical Research key player in Europe

This collaboration propels us from serving the Middle East and North Africa (MENA) to an expansive presence across Europe, the Middle East, and Africa (EMEA).

24 Aug 23

ISO 13485 Certificate for AL TIRYAQ

At AL TIRYAQ, we are dedicated to delivering the highest standards of quality and excellence in all aspects of our services. We're proud to announce that we have achieved ISO 13485 certification, underscoring our commitment to adhering to industry best practices and continuous improvement.

19 Aug 23

Registration of Medical Devices in Egypt

As a medical device manufacturer looking to access the Egyptian market, you must register your products with the Egyptian Drug Authority (EDA)

12 Jun 23

A Guide to ISO 13485:2016 compliant Quality Management System (QMS) for Medical Devices Stakeholders

These Guidelines applies to all clinical trials conducted in the United Arab Emirates. It does apply to interventional, non-interventional studies including medical devices.

27 Apr 23

Guidelines for Conducting Clinical Trials with Investigational Products and Medical Devices

These Guidelines applies to all clinical trials conducted in the United Arab Emirates. It does apply to interventional, non-interventional studies including medical devices.

26 Apr 23

Technical File Assessment (TFA) for Medical Devices in Saudi Arabia

These Guidelines applies to all clinical trials conducted in the United Arab Emirates. It does apply to interventional, non-interventional studies including medical devices.

admin

Subscribe to our newsletter