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Clinical Monitoring

Our clinical monitors are chosen for their experience in Clinical Research and the appropriate therapeutic area and also for their high level of commitment. 

Our clinical monitors are regionally based in order reduce travel costs and increase efficiency.

CROMSOURCE makes training a priority and all our staff undertake a specific and personalised training program. This means you can rely on the quality of clinical monitors assigned to your study. The CROMSOURCE network of monitors perform all activities related to pre-trial/qualification visits, initiation visits, interim monitoring visits and close-out visits, ensuring compliance to the protocol and all regulatory requirements. They also maintain strong and constructive relationships with investigative sites to ensure successful trial progress.

In addition to our full service offering, CROMSOURCE also provides teams of monitors to work under the Sponsor’s project management (our Managed Monitoring service).

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