Clinical Study Design
Service Description
Consulting on the design of a clinical protocol for the clinical evaluation procedure to collect clinical data in support to the certification process throughout the lifecycle of the medical device. Application of MDCG 2020-1 principles in the design of the specif clinical study; MDCG 2020-1.
Keywords: Clinical investigation, clinical study, clinical evaluation procedure, CE certification process
Offerings:
Research & Development
Conformity & Compliance (certification, audit, corrective and preventive action, documentation, gap & risk analysis, etc.)
Clinical Investigation Support (clinical studies & trials, coordination, design, feasibility, documentation, compliance, operations support)
TEF-Health Use Case Domain:
all
Provider & Contact
Provider Organisation
Politecnico Di Milano (POLIMI)
Provider Country
Italy
Published Email
tef-health@polimi.it
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.
Sign in or register to see pricingOperational Details
Service Inputs
Study Objective, Primary and secondary goals; Methods
Service Outputs
Report on the design of the clinical evaluation
Dependencies & Restrictions
MDR
Service Standards
EU Regulation 2017/745 , MDCG 2020-1
- EU Regulation 2017/745
- MDCG 2020-1