Our divergent team of chemistry and medicine assist Clinical Pharmacology Services, in providing safety and ethical solutions for Bioequivalence – Bioavailability studies are the hallmarks of our workforce.

With complete understanding of conducting a full extent of bioavailability / bioequivalence clinical studies in the generic product development process and approval pathways, gives confidence to our stakeholders that the outsourced project will be completely professional and with most prompt economic way possible.

The pharmacokinetic, bioavailability and bioequivalence studies are conducted in strict compliance with national and international regulatory guidelines that are monitored by independent quality assurance team. Within levels of management, team members take ownership of the project, providing clients with a more personalized, strategic approach to clinical management queries in the context of the phase, location and objectives of the study.