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Clinical Research Unit- Regulatory support

Physical
Unique Identifier: fb1cc937-9814-4aeb-800e-5582e91f21ea

Service Description

• Assisting SMEs in regulatory submissions in compliance with applicable laws and requirements • Providing SMEs with the necessary regulatory documents • Liaison with regulatory bodies: Ethics Committees (EC), National Agency of Drugs Safety (ANSM)

Offerings: Ethics & Regulatory Affairs (ethics board approval, legal requirements, ...) Clinical Investigation Support (clinical studies & trials, coordination, design, feasibility, documentation, compliance, operations support, etc.)
TEF-Health Use Case Domain: all
Provider Logo

Provider & Contact

Provider Country France
Published Email maryame.sy@ihu-strasbourg.eu

Pricing is available to registered users. SMEs receive significant state-aid reductions (GBER) — or, depending on the call, free services during the funded project. Sign in or register to see the price for your organisation.

Operational Details

Service Inputs Clincal protocol, specification
Service Outputs Draft for the regulatory and ethic approval