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.

Mr Praneeth Barra

Director - Business Development

Praneeth brings over 13 years of experience in business development, client relationship management, and strategic growth within the Clinical Research Organization (CRO) industry. His business development and client acquisition expertise spans a wide spectrum of CRO services across geographies. He has successfully supported global sponsors by aligning scientific, operational, and commercial strategies to accelerate their product development programs. 

With strong relationships across major international markets including the US, Europe, and Asia-Pacific, Praneeth has actively represented organizations at leading global industry conferences to foster strategic partnerships and strengthen client engagement. His broad exposure to end-to-end drug development environments empowers him to understand sponsor expectations and deliver high-quality, and regulatory-compliant solutions that drive both business and operational success.

 

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Location

Bangalore, India

Call Us

+91 80 45500700

Email Us

info@ivrs.org.in