iVRS

iVRS News

Successfully Completed 100 + Extractable and Leachable (E & L) Studies.

Extractable & Leachable Studies conducted at iVRS has been approved by USFDA and Health Canada.

In Vitro Release Test (IVRT) Studies conducted at iVRS has been accepted by Saudi Food and Drug Authority (SFDA).

Successfully completed PK based bioequivalence study of Cladribine in RRMS Patients for Jordan Food and Drug Administration (JFDA) submission.

Rich Experience in Handling Global Biosimilar Studies.

Successfully Completed Global Ophthalmology Device Study.

Our Process and Systems are ISO 9001 & ISO 27001 Compliant.

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Dr_Nagendra

Dr. Nagendra N MD, DNB, MBA

Chief Scientific Officer

With more than 15 years of experience in research and more than a decade in clinical research, has managed studies in all therapeutic areas. He has managed both global and local clinical studies. Vast experience of conducting clinical studies in US, Europe, middle east, south east Asia, Bangladesh and India.

He brings with him valuable experience both from the academics and Industry. He has worked in prestigious institutions like NIMHANS, Sri Jayadeva Institute of cardiology, CROs like Ecron Acunova, ClinTec International etc. He has successfully faced several regulatory and international sponsor audits and has mentored monitors in managing phase I to IV studies. He has worked closely with regulatory agencies across the globe.

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Location

Bangalore, India

Call Us

+91 80 45500700

Email Us

info@ivrs.org.in