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Investigational New Drug file (FDA in USA) Investigational Medicinal Product Dossier (EMA in Europe) : dossier submitted to health authorities in order to obtain the authorisation to launch the first trial on human (FIM: First-In-Man).

PhinC offering in the area includes:

Scientific & Regulatory Reporting

From the initial regulatory approval to the end of your development, you will require regulatory compliant documentation. But it does not end there! You will need to show that your project is secure and needs development. PhinC can help you to rise to this challenge.

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