The Clinical Research Secretariat (CRS) is a unique centre developed under TMC which serves as the

central contact point for all collaborative research projects within the institution. Any collaborative

study, whether investigator-initiated or part of a broader research network, must be submitted to

CRS for approval. The approval process follows a structured, three-tier system:

CAB Review: The CRS initially reviews the study and forwards it to the CAB for further assessment.

Scientific Committee Review: Once approved by CAB, the study is then sent to the Scientific

Committee for further review.

IEC Review : After Scientific Committee approval, the proposal is finally reviewed by the Institutional

Ethics Committee (IEC) for ethical clearance.

Additionally the CTA/MoU goes for review from the legal Team,TMH. Throughout this period, CRS

plays an active role in guiding researchers through each step, ensuring a smooth and efficient

approval process. CRS also facilitates investigator-initiated studies and thesis projects, supporting

academic and clinical researchers in advancing their work. Additionally, CRS is also involved in

training activities.