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With patient safety becoming an increasing focus of attention, the regulatory challenges in the Middle-East and North Africa are now more varied and complex than ever. The Pharmaceutical Regulations Summit features governments, regulatory authorities and expert insights from across the GCC and MENA to help you tackle and overcome these regulatory challenges, and ultimately help improve the drug, cosmetic and device approval processes for pharmaceutical, cosmeceutical, biopharmaceutical and medical device companies
From competent authority bodies on their interpretations of rules and guidelines.
In speed-networking and interactive exchange with 150+ of your peers including: regulators, directors and other compliance managers.
The most up-to-date knowledge of regulations, registrations and post-market surveillance of pharma, cosmetics and medical devices.
Directors, Managers & Practitioners from: Leading Pharmaceutical, Biopharmaceutical, Cosmeceutical and Medical Device Companies, as well as Regulators And Government Authorities responsible for:
Our interactive 4-day agenda kept attendees busy and engaged through a variety of sessions including...
Our insightful keynotes, panel discussions and expert insight presentations provided by the senior speaker faculty discussing pharmaceutical and medical devices regulations, registrations and submissions.
Our networking sessions ensured that attendees had a chance to have a quick initial meeting during the conference. Regulators, pharmaceutical regulations and compliance professionals and consultants were introduced, ideas were shared, business propositions discussed, and valuable relationships created through over our speed-networking sessions, one-to-one meetings and closed sessions.
Interactive pre-event workshop on eCTD implementation and submission, a Focus Day on Medical Devices, as well as in-depth sessions covering the whole regulation spectrum from pricing to market access, classiﬁcation, serialisation, pharmacovigilance and more.