Regulatory Affairs, Compliance with local regulations, Project management, Knowledge of Asia Pacific countries IVD standards and regulations, Problem-solving, Product registrations

Iso 13485, Design Dossiers, regulatory strategy, FDA product registration, Vigilance reporting, EU MDR, Global registrations, Technical Files

team effectiveness , Time Management, Nutrition, Bilingual, Attention To Detail, Chemistry, Regulatory Affairs, Regulatory Requirements, Surveillance, health sciences, Regulatory Compliance, Able To Work Independently

regulatory intelligence , Regulatory Affairs, ASEAN CTD, regulatory risk assessments, strategic regulatory advice, ectd

product registration requirements in Southeast Asia, regulatory affairs background, knowledge of Southeast Asia countries IVD standards regulations

Quality management processes, Iso9001, Regulatory Affairs, Regulatory Submissions, Gmp, IVD devices, ISO13485