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.

iVRS-Logo_resized-187x300 (3)
Consulting Services - Biopharmaceutical Services

Biopharmaceutical Services

iVRS support pharmaceutical product development by providing consultation with respect to review of clinical study data, formulation data including dissolution data etc. Also, iVRS can assist in designing the clinical studies for successful product development. iVRS also can develop IVIVR/IVIVC for appropriate pharmaceutical products to support product development and regulatory submissions.

Subsribe To Our Newsletter

Stay in touch with us to get latest news and special offers.

Address

Bangalore, India

Call Us

+91 80 45500700

Email Us

info@ivrs.org.in