Regulatory Services
Protocol Development
Project Management
Clinical Monitoring
Clinical Trial Supply Management
Site Management
Quality Assurance
Medical Monitoring
Data Management
Medical Writing
Medical Monitoring  
Our medical monitors come from experienced medical background.

They are able to apply their practical knowledge and clinical experience to present solutions for the issues occurred during the conduct of the clinical trial.

Medical Monitors work as per the ethical guidelines for the safety of the subjects and document and communicate the AE and the SAE occurred during the trial to the regulatory agencies, sponsor and the IEC within the stipulated time frame.
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