Welcome to iVRS, a Contract Research Organization (CRO), provides full service in vitro solutions in pharmaceutical product development. Our services in the area of in vitro characterization and in vitro bioequivalence studies of pharmaceutical products are guided through systematic R&D, strict regulatory standards and quality & compliance. iVRS comprises an experienced team in the area of in vitro bioequivalence studies, bioequivalence/clinical research, pharmaceutical development & dissolution development and acquired a thorough understanding of regulatory requirements in these areas. iVRS team believes in systematic and continuous training for operational excellence. iVRS comprises experienced team of scientists (combined experience 100+ years) in the area of analytical and clinical studies for pharmaceutical development. The team experienced in designing, executing and submitting analytical (including Extractable and leachable, IVRT & IVPT, Feeding tube) & IVBE studies to regulatory agencies. iVRS aspire to include every in vitro techniques adopted and recommended for various pharmaceutical dosage forms including oral solid/liquid dosage forms, injectable suspension/solutions, ophthalmic suspensions/solutions/drops, pulmonary aerosols/sprays, dermal products like ointments/creams/gels etc, suppositories/vaginal preparations etc. iVRS believes in thorough, methodical, appropriate research and development in method development, validation and optimization of in vitro techniques and analytical techniques. iVRS meticulously follows the regulatory standards like good laboratory practices, good clinical practices, good documentation practices, applicable regulatory guidance, ICH guidelines with adherence to quality & compliance, synchronized with R&D, study conduct and appropriate presentation of data, would lead to faster and easier review by regulatory agencies. iVRSteam relies on systematic and continuous training, which is key for the operational excellence.