Medical Device Documentation, Regulatory and Marketing Support Specialist
Singapore
Malese, Indonesiano, Inglese
Alcune informazioni sono riportate in lingua inglese.
Chi sono
I’m a freelance medical device regulatory and documentation specialist with experience in ISO 13485 QMS, ASEAN regulatory requirements, and product registration in Malaysia, Singapore and Indonesia. I support MDA, HSA and Regalkes registrations, technical files, dossier preparation, regulatory gap reviews, product classification, and ISO 13485 documentation. I can also create and improve medical device presentations, brochures, training materials, technical content, and professional Word, PowerPoint, and PDF documents.... Continua a leggere