Dissolution Experts.

Our DNA is in-vitro dissolution testing. Being the only Contract Research Organisation (CRO) with a dissolution testing speciality, our team has a track record of successfully determining the best approach for a wide range of products, including implants, semi-solids, tablets, APIs, and many more.

Beyond Dissolution.

In-vitro dissolution testing has been Ortiv-Q3's area of expertise since 2019, however the company offers much more than "just" dissolution-related services. Our teams are proficient in many analytical techniques and have access to cutting-edge instrumentation for a wide range of test types, including stability testing and API characterization.

Quality System.

In accordance with US 21 CFR Parts 210, 211 and the guidelines of ICH Q10, the management of Ortiv-Q3 Research is dedicated to putting into place a Pharmaceutical Quality system that satisfies the relevant Good Manufacturing Practices criteria. Ortiv-Q3 Research is dedicated to the highest standards of professional conduct and customer service, utilising established protocols, techniques, and skilled and productive staff to deliver dependable, high-caliber outcomes on schedule.

DOWNLOAD AREA

In addition to Ortiv-Q3 in India, SOTAX has two other laboratories in Europe and the USA, all based on the same proven quality management system and offering first-class services in a GMP-certified and FDA-approved environment. Throughout the whole life cycle of your products, our local experts can help you, whether you need assistance with technological development or want to outsource regular testing.