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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P Prasad Rao

Has been associated with sales, marketing and business development in the pharma industry for more than 3 decades out of which the last 17 years have been in clinical research. In his last assignment, he was heading Business development and Project Management with one of India’s leading CRO.

He has connections with clients in all major markets and has travelled to more than 20 countries. He has attended many global industry meets to enhance industry contacts and grow business. Before being associated with clinical research, he was in pharma marketing for 18 years.

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Location

Bangalore, India

Call Us

+91 80 45500700

Email Us

info@ivrs.org.in