About Us

Longfort Consulting provides regulatory expertise to secure clinical trial approval in a timely and quality-controlled manner.

Leverage our guidance in oncology, immunotherapy, rare diseases, pediatrics and gene therapy to achieve successful trial outcomes.

Conduct robust clinical trials using watertight protocols and a purpose-built document package to obtain first-pass approval from regulatory authorities.

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Services

Turn regulatory complexity into speed. Agile expertize tailored for Biotechs, MedTechs and academia.

Regulatory Strategy

Submission & CTIS expertise

Agile Operational Support

Are you ready to streamline your submission ?

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Longfort Consulting - Toulouse, France

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