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Clinical Monitoring
Clinical Monitoring

Our Clinical Research Associates (CRAs) are appropriately qualified and industry recognized for their outstanding reputation in customer service, in-depth knowledge of industry regulations and guidelines, and therapeutic knowledge. They ensure compliance with protocols, quality standards, data collection, and regulatory guidelines. The CRAs are regionally located across North America, reducing travel time and expenses. Our CRAs enjoy their profession, which we feel is ultimately reflected in their interactions with clients, colleagues and site staff as they perform their duties.

 
Our services include:
Site selection, initiation, interim monitoring, and close-out
Site personnel training, mentoring, and guidance
Assessing protocol compliance and data integrity
Regulatory document review
Pharmacy training and drug accountability
Ensuring GCP, consenting, confidentiality, and safety requirements are met
 

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