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France Pharmaceutical Regulatory Affairs Consulting

You can trust the Pharmassent services for your medical product development plan for the European market. We help pharmaceutical laboratories and biotech companies manage the product regulatory authorization process, market access, reimbursement procedures, R&D financing, drug manufacturing, marketing…

Pharmassent is experienced in implementing high-quality assessment of any project to audit and build a strong strategy to target the French market.

Our consultants have wide scientific background and excellent technical knowledge of regulatory affairs to suggest procedures for optimised efficiency.

You can rely on our expertise to get your products (drugs and/or medical devices) to the French market faster with an appropriate tailored solution.

"Pharmaceutical Business Strategy And Authorization Procedures To Successfully Achieve Your Goals"

Pharmassent is a consultancy firm specialized in strategic pharmaceutical business development with strong proficiency in France and Europe. By concentrating intensely on France and ANSM French pharmaceutical regulatory authorities as a gateway to all Europe, we offer the knowledge, skills and strong experience in the pharmaceutical industry to get your product to market. We offer specific and unique quality advice. We support multinational and smaller manufacturing companies. Our agency can be a very reliable and efficient partner in your product submission (drug and/or medical device), marketing authorization process, reimbursement procedures, R&D financing, drug manufacturing, product marketing and sales, fundraising, hospitals tenders or navigating regulatory issues for product approval

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Specialists in Health products with many years experience. Please read more about our many consulting services below.

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