REGULATORY MEDICAL WRITING

CHEMISTRI

We are involved in a broad spectrum of tasks, trained on the latest global regulatory requirements, and part of an internal and external team. It is ourgoal to write complex and highly scientific documents in several therapeutic areas in a transparent manner to enhance the drug submission process.

These documents may include, but are not limited to: clinical study reports, clinical study protocols, Investigator's Brochures, informed consent forms, briefing documents...

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