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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Medical Writing

We understand your need for fully integrated clinical study reports, incorporating all investigator and sponsor requirements, while still adhering to regulatory requirements. Our medical writers have considerable experience in writing these documents and presenting your data effectively and on time.

Our in-house medical writers are involved in the study through every stage to ensure a comprehensive understanding of the study – consequently our protocols and clinical study reports are insightful and accurate. Delivery of your final, summarized data will be presented in paper copy as well as password-protected electronic files. At the end of the study, we can also provide a full report containing all information ready for submission.

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Address

Bangalore, India

Call Us

+91 80 45500700

Email Us

info@ivrs.org.in