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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IVRT/ IVPT Studies (Franz Diffusion Technique)

iVRS offer method development, validation and testing services according to FDA, European guidelines and other applicable guidelines. IVPT study involve skin percutaneous absorption and permeation kinetics determined by drug permeation parameters including rate and total amount permeated. This
technique can be applied for topical/transdermal drug permeation evaluation and bioequivalence studies.

iVRS also offer invitro release tests (IVRT studies employing artificial membranes) using franz diffusion cell technique for various dosage form as per various regulatory requirements

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Address

Bangalore, India

Call Us

+91 80 45500700

Email Us

info@ivrs.org.in