Regulatory Affairs Intern/ Thực Tập Sinh - Đăng Ký Sản PhẩmCÔNG TY TNHH TRANSMEDIC

Be responsible for compliance and product registration (medical device, health supplement, cosmetic and medicine). A&P registration and make price disclosure.
Maintain and track the registration status of all marketed products.
Maintain data in information systems or databases, coordinate regulatory documentation activities, regulatory documentation database on the server.
Research, translate the documents for registration dossier.
Review and update information regarding documents for submission as requires for regulatory compliance liaise with competent authorities.
Provide and support documents for marketing purpose.
Provide technical review of data or reports
Study clinical & legal document & relevant regulations to assist job.
Other tasks are assigned by Line manager.