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Clinical Research Services: clinical operations set-up

Physical
Pricing/Discount Options: Call #2
Unique Identifier: f713bc03-80ef-4a9a-aeaa-4e2fe705472d

Service Description

Clinical investigation set-up with patient inclusion, patient follow-up, data collection, queries management, ...; clinical investigation coordination (mono-centric or multi-centric); the hospital may be the sponsor or an associated investigation center.

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

Provider Country France
Published Email tef-health@chu-rennes.fr

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 The clinical protocol has been authorized by the French national regulatory authorities (Ethical committee and/ or ANSM and/ or CNIL). The project mangement plan has been written
Service Outputs Last patient, last visit; Clean database
Dependencies & Restrictions Authorized protocol
Service Standards EU Regulation 2017/745; Good Clinical Practise; European Clinical Research Infrastructure Network (ECRIN) label
  • EU Regulation 2017/745
  • European Clinical Research Infrastructure Network (ECRIN) label
  • Good Clinical Practise