Luis Everton Esmeraldino

Luis Everton Esmeraldino has a long history of work experience in the pharmaceutical and healthcare industries. Luis Everton began their career in 2003 as a Consultor for ANVISA. In 2006, they became a Regulatory Affairs Coordinator for Zodiac Produtos Farmacêuticos. During this time, they were responsible for certification of good practices for manufacturing and control of medicinal products, contracting and performance of bioavailability test and pharmaceutical equivalence, and management of the regulatory team. In 2008, they joined Biophytis - New Therapeutics for aging diseases as a Regulatory Affairs - Pharmacist. In this role, they managed food research and development projects with functional claims, conducted clinical research, and was responsible for quality control and quality assurance, certification, and registration of products at ANVISA. In 2010, they moved to GSK as a Regulatory Affairs Executive. Luis Everton was responsible for registration and post-registration of medicines with ANVISA, registration of active pharmaceutical inputs (IFA) and GMP certification with ANVISA, and coordination and planning of GMP certifications of international plants. In 2013, they became a Consultor for VISALEEX and a Farmacêutico Proprietário for Apotheke. Finally, in 2020, they joined Biophytis - LIVE HEALTHIER LONGER as a Clinical Operations Manager LATAM and Regulatory and Clinical Affairs Coordinator LATAM.

Luis Everton Esmeraldino attended the Universidade Federal de Santa Catarina from 1992 to 1995 and obtained a degree in Farmácia. Luis Everton then went on to attend the USP - Universidade de São Paulo from 1996 to 2003 and obtained a degree in Fármacia from the Faculdade de Ciências Farmacêuticas de Ribeirão Preto. Additionally, they have obtained certifications for Doutorado and Mestrado from the Faculdade de Ciências Farmacêuticas de Ribeirão Preto - USP.