About us

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.

ARIRDMSCRO Doctrine

Pledge:

We pledge to adhere, to perform all our study specific actions or activities with adherence to our aim to transform results with high successful accomplishments of actions.

We value challenges because they produce innovations. We commit to approaching problems with enthusiasm and optimism.

Philosophy:

Our philosophy is to be a company, which is driven by a system of motivating concepts and principles. We are dedicated to meet our Client’s business needs with a constant pursuit to leverage our excellent services. Our firm believe and strongly adhere in our company values, guides us to live and work at ARIRDMSCRO.

Team Work:

We work as one team with our business partners in a spirit of trust and cooperation. Teamwork is one of our core principles which is mingled by cooperative efforts of our employees along with our vendors striving to achieve a common goal of delivering solution centric methods, to embark upon quality driven and regulatory compliant clinical trials.

 

Communication:

One of our foundation pillar is openness in communication. At ARIRDMSCRO, we are oriented to our commitment to work ethically. All our employees are important assets for us and we all thrive on our individual efforts to ensure high quality work standards which are backed by our internal locus of our actions.

 

Accountability:

We focus to complete clinical trials projects with full accountability to our values and commitments.

History:

Established as a pharmaceutical contract research organization company in April 2020 – ARIRDMSCRO has been providing contract clinical research services since inception.

We have been involved in clinical trials across Phase I to IV, for therapeutic areas such as Infectious diseases (COVID–19).

Our founding member, has wide variety of experience in innumerable therapeutic areas of clinical trials.

ARIRDMSCRO aims to offers Drug/Device clinical trial management consultancy services for global blue-chip, as well as for emerging pharma/bio-tech companies based at US, CANADA, EU, ANZ, Japan, MENA, LATAM and India.