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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At iVRS, we’d like to stay on top of the latest in our industry to bring you the best of services and solutions. If you are looking to be updated on the latest developments and innovations in the Clinical Research industry, watch this space. We’re launching our content initiatives just for you!

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If you are an organization looking to engage a diligent, effective and reputed clinical research organization, you’ve
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speed and efficiency in your research requirements.

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