Monitoring activities conducted by Clinical Cert Clinical Research Associates (CRA) are regarded as one of the most important part in the conduct of a new drug development. Our CRAs are skilled and well trained to ensure a highest quality review of your study data and to interact effectively with the study sites.

Being the main communication link between site and study sponsor the main tasks of Clinical Cert CRAs during a clinical study site visit are:

Establishing a clear, individual and well-structured communication to the site
Ensuring the regulatory compliance of study sites
Overseeing the process of data collection
Verification of source documents and case report forms
Resolving of queries

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