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Regulatory Consultancy

Regulatory Consultancy

Reviewing documents prior to regulatory submission, writing summaries of M&S work. Exprimo consultants can participate in mock advisory committee meetings. Exprimo has extensive regulatory experience and several of our consultants have accompanied drugs to market.

Among Exprimo’s spectrum of regulatory consultancy services are the review of regulatory documents intended for submission, writing parts of modules of the CTD with focus on modeling and simulation, and participation in regulatory committee meetings throughout drug development and submission. Several Exprimo employees have experience in accompanying drugs from Phase 1 all the way to market.

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