Section 1: Company Information 1 Company Information
Tell us who you are and where the company is based.
Section 2: Product Information 2 Product Information
Describe the product or technology and what it is used for.
Product / technology name *
Product category * Select an option Rehabilitation Recovery Diagnostics Digital Health Home Care Monitoring Surgical / interventional device Hospital equipment Other medical device
Short product description
Target indication / use case
Current development stage * Select an option Concept / prototype Preclinical validation Clinical validation CE marked FDA cleared / approved Commercially available Revenue generating
Section 3: Evidence and Regulation 3 Evidence and Regulation
Where the product stands on regulatory approvals and clinical evidence.
Current regulatory status * Select an option CE marked UKCA marked FDA cleared / approved In clinical trial Not yet approved Other
Clinical evidence available * Select an option Published clinical study Clinical trial data Real-world evidence Pilot hospital data Usability data No clinical data yet
China regulatory status Not provided No China activity yet Early discussion Local agent identified NMPA pathway assessed NMPA submission started Already approved in China
Section 4: China Interest 4 China Interest
What you are looking for in China and your preferred entry path.
Section 5: Files and Consent 5 Files and Consent
Optional supporting links, and how we may use your submission.