We are a Clinical Services Company for the Pharmaceutical Industry, unique in Argentina for the exclusive specialization of its services in conducting Pharmacokinetic Studies, Phase I, Bioavailability and Bioequivalence.
Since 2001, with a recognized track record in the Pharmaceutical Industry, we provide the Local Industry with Clinical, Pharmacological, Regulatory, Analytical and Statistical Services for conducting Bioavailability and Bioequivalence studies for generic products.
Learn moreWe offer a wide range of services to support the development of your products before and during their commercialization.
Conducting Phase I to IV studies with the highest quality standards.
View detailsLeaders in Argentina in the design, execution and analysis of BA/BE studies.
View detailsGood Pharmacovigilance Practices program under ANMAT regulations.
View detailsOur Research Unit is equipped to meet the growing needs of clinical research based on international good practice standards.
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On 01/20/2026, ANMAT Salud published Disposition 47/2026 in the Official Gazette, updating the list of APIs that must undergo bioequivalence/bioavailability studies.
Read moreDr. Ethel Feleder, our Director, was selected by ANMAT to join the Network of Experts in Pharmacological Clinical Research.
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