Our quality control staff are rigorously trained in the application of Good Laboratory Practices, Good Documentation Practices, and Good Clinical Practices to ensure that clinical and analytical research and applicable regulatory requirements are conducted in strict accordance with the current regulations.
Bioequivalence and biocomparability
We comply with national and international requirements to run the necessary Dissolution Profile and Bioavailability/Bioequivalence studies to demonstrate the interchangeability of generic drugs.
Stage studies
We have an expert team capable of designing a complete study, managing it, monitoring it, and delivering the results in a timely manner.
Regulatory approach
Aligned with the guidelines issued by the Research Ethics Committee and the Research Committee of INCan, our team promotes effective solutions in compliance with the regulation, to design and carry out clinical protocols that correctly guide the development of new drugs, for the benefit of our patients.
Drug surveillance
From a patient-centered ethic, we perform clinical monitoring of the mechanism of the new substance marketed, in order to locate effects and present results in compliance with the regulation.
Pre-clinical
We are involved in preclinical studies to contribute to the evaluation of the safety and efficacy of biotechnological medicines and other health supplies, based on applicable regulations.
Specialized Research Services
Liquid Biopsies. microscopy. mass spectrometer.
