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Veeda has a vast expertise in the field of Clinical Research. We place a firm emphasis on our scientific knowledge and our past experience to plan the conduct of each clinical trial in advance. This enables us to provide quality results on time in each trial. We also follow a stringent quality check to assure no statistical errors in our final results.
Our senior teams leading various departments have a combined experience of over 100 man working years in the Pharmaceutical Companies and CROs together. With the help of this expertise, we offer our services in exploring Bioavailability / Bioequivalence studies in Healthy volunteers as well as Patients, and Phase 1,2,3 Clinical trials. Our Board has a unique blend of experience and expertise in exploring western world's research which enables us to offer the whole spectrum of Biosimilars and Biologicals clinical development. Due to our subject matter expertise, we are pioneers in offering speciality services like Central Bioanalytical Laboratory services, Biopharmaceutics Services, Quality Assurance services and Project Management Services.

Our exemplary regulatory track record

33 times
7 times
5 times
3 times
1 times
South Africa - MCC
1 times
NPRA - Malaysia
4 times
13 times