Medical Device Registration and Approval Process for the Pacific Rim (including India, Japan, China, Singapore, Australia, Taiwan, Hong Kong, and other locations) 2017 is a conference that covers topics such as:
- Are medical devices required to be registered before they can be sold?
- Which regulatory bodies are responsible for medical device registration in each country?
- What are the different application categories for medical device registration?
- What are the different regulatory classifications for medical devices?
- What are the document requirements for notification for the various classes of medical devices?
- What does the registration pathway look like for each regulatory classification?
- Is local testing (type testing/sample testing) required for registration?
- What are other requirements that are necessary for approval in addition to the device application?
- Is approval in the Country of Origin required for registration?
- When are clinical studies required for registration?
Medical Device Registration and Approval Process for the Pacific Rim (including India, Japan, China, Singapore, Australia, Taiwan, Hong Kong, and other locations) 2017 brings together:
- Clinical Project Managers
- Clinical Research Associates
- Clinical Investigators and Clinical Research
- Regulatory Affairs Professionals
- Regulatory Affairs Specialists
- Regulatory Affairs Management
- Auditors
- Regulatory Project Leads/SME`s
- Clinical Affairs
- Compliance Specialists
- Consultants
- Quality Assurance
- Distributors
