We are an end to end service provider CRO in India. Our rich and diverse experience enable us to carry out multiple clinical trials studies in different phases with various clients. We have constantly leveraged our quality driven, cost focused and regulatory compliant clinical studies for our client’s. Ensuring our relentless commitment to our diverse ever-growing drug & medical devices clinical studies management portfolio.

ARIRDMSCRO owner, Mr. Prateek Mehra is responsible for all operations of the firm. Mr. Mehra holds a M.Sc. in Medical Microbiology and has a vast experience of 19 years of Clinical research industry. His rich and diverse experience includes, Global Clinical Project Management, Clinical Operations Management, Complete Clinical Trials global team management, complete clinical trials with drug or medical devices, development portfolio magement. He has extensively worked with Investigator Initiated studies and registry studies portfolio. Has managed complete reporting responsibilities for global clinical trials in drug/medical devices management, across numerous therapeutic area’s within large and complex organizations matrices. During his tenure, Mr. Mehra has managed large clinical studies and innumerable vendors in different geographies, on global clinical trials in alignment with various pharmaceutical/bio-tech companies. He carries a rich understanding of all clinical trials phases and strives to build ARIRDMSCRO a solution centric approach for all clients.