Assessoria Czm

CZM Regulatory Consulting is a specialized consultancy in regulatory affairs, data management, and technical compliance, with over 15 years of experience supporting pharmaceutical, cosmetic, and food companies. Founded by Camila Zago, a pharmacist and regulatory affairs expert, CZM was created to simplify processes and ensure full compliance with ANVISA, local health authorities (VISA), and international agencies. We work in close collaboration with Regulatory Affairs, Quality, Pharmacovigilance, Clinical Research, Legal, Pricing, and Marketing teams, providing both strategic and operational regulatory support. CZM has extensive expertise in preparing, reviewing, and structuring regulatory dossiers, both in CTD (Common Technical Document) format and in customized formats requested by clients, ensuring accuracy and alignment with ICH guidelines and ANVISA requirements. Our team also authors CMC (Chemistry, Manufacturing and Controls) sections and develops high-quality CMC written documentation with technical depth and regulatory clarity. We provide regulatory data management and validation across systems such as VEEVA/RIM, RAS, SHARE, and UltraReg, including version reconciliation, document digitization, and technical support for publication and submission. We combine technical excellence, agility, and confidentiality to deliver tailored regulatory solutions that help clients achieve compliance and efficiency.