We provide training in clinical research and medical writing.
The team provides training program on all aspects of drug development and research activities to the various stakeholders in clinical research and drug development. The key areas covered include:
● ICH GCP guidelines
● Drug development process
● Clinical research
● Audits and inspections
● Ethics Committee and investigators responsibilities
● Roles and responsibilities of CRC (Clinical Research Coordinators)
● Regulatory laws and guidelines – global and Indian
● Recent amendments and revisions.