Life Sciences Regulation in United Arab Emirates: Overview

Practical Law Country Q&A 4-636-6091 (Approx. 14 pages)

Life Sciences Regulation in United Arab Emirates: Overview

by Melissa Murray, Bird & Bird LLP
A Q&A guide to life sciences regulation in the United Arab Emirates (UAE).
This Q&A provides a high-level overview of key practical issues, including life sciences clinical trials, manufacturing, marketing, abridged procedure, pharmacovigilance, data privacy, packaging and labelling, biological medicines, medical devices, health care IT, combination products, borderlines, and natural health products.

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Resource ID 4-636-6091
Copyright © Thomson Reuters Canada Limited or its licensors. All rights reserved.
Law stated as at 01-Jul-2023
Resource Type Country Q&A
Jurisdiction
  • United Arab Emirates
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