Site / Investigator

Staff support and Project management:

AMRs provides the site and the investigator with trained and qualified staff to assist and handle the project as per the protocol and delegated responsibilities. The team ensures that all requirements as per applicable SOPs are met and trial is executed as per the approved protocol.

SOP Writing:

Standard operating procedures (SOPs) are the guiding documents required by all sites for the conduct of research activities as per the standard set by the institute and regulatory authorities. SOPs act as a reference document to ensure uniformity in the activities conducted by all departments, staff and site as a whole. The main purpose of a SOP is to specifically prevent procedural deviations by outlining prescribed processes. AMRs helps in preparing site specific SOPs to meet all requirements and ensures adherence to the same.

Academic clinical trial support:

AMRs also assists the Investigators in conducting Investigator Initiated trials/Academic clinical trials.