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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Board of Directors

"One of the core strengths of iVRS, is our ability to bring together talent, technologies and industry’s best practices & processes that assure generation of high quality data which can then be transformed into actionable information, to enable our customers to file dossiers to the authorities in a timely manner."

- Umesh B A

"We are on a mission to bring reliable and accurate clinical research services to the industry and in doing so, bring credibility and accountability to companies and brand-owners, while improving safety for the consumers."

- Rashin Subbaiah

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Location

Bangalore, India

Call Us

+91 80 45500700

Email Us

info@ivrs.org.in