Clinical Sites

Each Clinical Trial Site must apply to the Network and fulfil basic requirements such as dedicated space to perform clinical trials, qualified and experienced personnel, experience of multicentric clinical trials and to agree to implement organizational Standard Operating Procedures (SOPs) according to ICH GCP Guidelines.

 

Each Clinical Site will be submitted to an On-Site Evaluation Visit by independent auditors and should agree to implement the necessary actions in order to become a certified Clinical Site of Excellence of the EVICR.net Network.

 

How to apply as a Member
Please download here the EVICR.net and Steps for Memberships.

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