Clinical Research Regulatory Affairs

• Documentation & Review
• CTA submission
• Clinical trial approval
• Adverse event reporting
• Statistical Analysis & Interpretation
• Import and export licensing.
• Annual report submissions.
• Site approval & licensing

CRO-India works adjacent with sponsor to help him follow all the trial related regulatory dealings. CRO- India work close with sponsored Clinical trials to grasp all the factors affiliated to the research and thus facilitates the better regulatory proceedings for the sponsors. This not only saves time but also let research work and process smoothly.

To know more about our collaborations and regulatory consulting mail us at contact@cro-india.com