Carlos Leandro

He has hands-on experience detecting adverse drug reactions, preparing regulatory dossiers, and overseeing medical device safety through technovigilance and pharmacovigilance reporting. Carlos is skilled in navigating both local and international regulations, including those established by COFEPRIS, the FDA, and the EMA, for both medical devices and pharmaceuticals. His background also includes experience with high-cost medicines, controlled substances, and cold chain medicines.

Prior to joining Pure Global, Carlos held positions at DEWIMED SA and Hospital Star Médica Hip. He holds degrees in Pharmaceutical Chemistry and Biology from Universidad La Salle in Mexico.