Regulatory Services
Protocol Development
Project Management
Clinical Monitoring
Clinical Trial Supply Management
Site Management
Quality Assurance
Medical Monitoring
Data Management
Medical Writing
Clinical Monitoring  
Each CRA at Asiatic brings a wealth of monitoring experience. Our lead CRAs develop and manage highly functional sites across India. Our CRAs help in communication between the sponsor and principal investigators through out the clinical study. Our CRAs conduct continuous on-site monitoring, training for the CRCs and the co-investigator.
Our Capabilities Include
Identification and selection of study specific investigators
Identification and management of IRB/IEC
Regulatory document review and collection
Site contract, budget negotiation and grant administration
On-site training
Site qualification, initiation, and closeout
Interim site monitoring
Drug accountability
Data query resolution
Quality control of the data generated
Communication with the sponsor and the sites for all the updates during the study
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