Murilo Rodrigues

Murilo Rodrigues has extensive experience in regulatory affairs and business development within the pharmaceutical industry, currently serving as Regional Business Development Manager and Regulatory Affairs Director at Chemo since May 2015. In this role, Murilo promotes strategic regulatory directions for Brazil concerning Active Pharmaceutical Ingredients (API) and Finished Dosage Formulation (FDF) from various international manufacturing sites, while providing regulatory support throughout the dossier submission process to ANVISA. Previous positions at Chemo include Regulatory Affairs Manager, Coordinator, and Analyst, focusing on registration activities and regulatory strategy development. Prior experience includes a role as Registration Trainee at FERST Consultoria, Pesquisa e Desenvolvimento for pesticide product registration, and a Product Safety Intern position at Syngenta, supporting toxicological studies. Murilo holds a degree in Pharmacy - Biochemistry from USP and a Specialist degree in Regulatory Affairs in the Pharmaceutical Industry from ICTQ.