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Our experts’ regulatory intelligence allows you to determine the requirements for the various aspects of drug development and clinical trials.

We base our advice on years of experience regarding pitfalls in strategic decision-making, interactions with Health Authorities, and the process of gaining local or global market approval. We can advise you when to start the dialogue with Health Authorities, facilitating the actual agency interaction, with you or on your behalf. We have hands on experience in a wide variety of indications and registration procedures, regulatory intelligence that we will leverage to determine the best regulatory strategy for your product. Our regulatory intelligence can give you the edge over the competition.

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Elise Destrée

Managing Consultant, Regulatory Affairs

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