Services – Teriaqi for Regulatory

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What We Offer

Services

We provide services in the medical field in the Kingdom of Saudi Arabia, providing medical drugs and medical preparations

Medical Device Importation License (MDIL)

The purpose of this document is to define and clarify requirements for

Medical Device Establishment License (MDEL)

The Medical Device Establishment License (MDEL) is a regulatory

Authorized Representation (AR)

Authorized Representation (AR) refers to a Saudi-based entity that has entered into a contractual agreement

Medical Device Marketing Authorization (MDMA)

A mandatory requirement for manufacturers of medical devices and IVDs when registering their products by the Authority.

Product Classification Application on PCS

Product classification is essential for medical device manufacturers who are looking to introduce their products into the Kingdom....

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Your guide to achieving compliance with regulatory standards efficiently

Taryaki includes a cadre of experienced experts with specialized experience and knowledge in regulatory affairs and registration of medical devices and laboratory devices with the Saudi Food and Drug Authority, headquartered in Riyadh, Kingdom of Saudi Arabia.

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Address Riyadh, SAUDI ARABIA

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