In this webinar, the speaker will discuss the updated differences in regulatory frameworks (regulatory requirements and compliance) in Asia, intending to help you understand and accurately interpret applicable laws and regulations governing medical devices in China, Hong Kong, Japan and Korea. This webinar will help you expedite the registration process for your devices in these Asian countries.Areas Covered in the Session :Updated medical device laws and regulations in China, Hong Kong, Japan and Korea.Definitions, Device classification and rulesRegulatory framework for medical devices in China, Hong Kong, Japan and Korea.Regulatory requirements for medical devices including in vitro diagnostic devices in China, Hong Kong, Japan and Korea.How to identify and address the regulatory requirementsHow to establish and maintain systematic methods to meet the regulatory requirements.How to streamline the regulatory process.Suggestions for best practices in a PASS-IT mannerInteractive Q&A sessionWho Will Benefit:Regulatory Affairs Managers, Directors and VPsClinical Affairs Managers, Directors and VPsQuality Managers, Directors and VPsQuality Managers, Directors and VPsCompliance Managers and DirectorsSales and Marketing Managers, Directors, and VPsComplaint Handling and Risk Management Managers and DirectorsSite Managers, Directors, and ConsultantsSenior and Executive ManagementCompliance Officers and Legal CounselBusiness Development Managers, Directors, and VPsPrice Tags:LiveSingle Live : For One Participant$ 249Corporate Live : For Max. 10 Participants$ 899RecordingSingle REC : For One Participant - Unlimited Access for 6 Months$ 299For more information and enquiries contact us atCompliance Trainings5939 Candle brook Ct, Mississauga, ON L5V 2V5, Canada  Customer Support: 416-915-4458