In Vitro Bioequivalence Studies
iVRS provides cGMP support for appropriate techniques to meet the USFDA requirements for in vitro bioequivalence testing of a variety of dosage forms. Combined with an excellent regulatory record, iVRS is better choice for a partner in testing for approval of new generic drug products requiring in vitro bioequivalence testing. Our experience in In Vitro bioequivalence testing includes following binding studies
◘ Sevelamer Carbonate
◘ Sevelamer Hydrochloride
◘ Calcium Acetate
◘ Lanthanum Carbonate
◘ Ferric Citrate
◘ Sucroferric Oxyhydroxide
◘ Patiromer
◘ Bile Acid Binders
◘ Colesevelam, Cholestyramine
◘ Colestipol
Others:
◘ Sucralfate (Bile Acid Binding, Albumin Binding & Pepsin Activity)
◘ Developed Methods for Sucralfate IVBE
◘ Quantitative Capsule Rupture Test (QCRT) Studies
(Omega 3 Fatty acid ester, ergocaliferol, etc.
Let us talk
If you are an organization looking to engage a diligent, effective and reputed clinical research organiztion, you’ve come to the right place. In Vitro Research Solutions was set up to help organizations like your’s achieve integrity,
speed and efficiency in your research requirements.
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Address
Bangalore, India
Call Us
+91 80 45500700
Email Us
info@ivrs.org.in