Regulatory Affairs

Regulatory affairs constitute an important role in the healthcare industry. Healthcare products, including pharmaceuticals, dietary supplements, diagnostics kits, medical devices and disposables require prior licensing from the UAE Ministry of Health to import, market and distribute products.

Our dedicated Regulatory Affairs Department undertakes the responsibility of complying with the Ministry’s regulatory requirements, assisting our partners to prepare all the documents required for registration and fulfilling our partners’ objectives by ensuring timely approvals.

As Ministry regulations are constantly evolving, IDS keeps abreast of this rapidly changing regulatory environment in the UAE. Our Regulatory Team brings a wealth of regional knowledge and industry expertise to ensure that our partners’ products meet all the updated registration guidelines.