The 93rd China International Medical Equipment Fair (CMEF) has successfully concluded. Over the four-day exhibition, GRZAN Group Limited had the pleasure of meeting with numerous industry professionals, partners, and clients, engaging in productive discussions and receiving valuable recognition, feedback, and new cooperation opportunities.
Throughout the exhibition, our booth remained a vibrant hub for technical discussions and regulatory consultations. Every conversation, every business inquiry, and every expression of trust strengthened our commitment to providing professional global medical device regulatory services and supporting manufacturers in expanding into international markets.
During the exhibition, the topics most frequently discussed with visitors included:
- Target market overview and regulatory landscape
- Product risk classification, predicate devices, and registration unit assessment
- Selection of the most suitable registration pathway and opportunities to shorten approval timelines
- Registration prerequisites
- Registration procedures
- Technical documentation requirements
- Labeling compliance requirements
- Registration timelines
- Registration fees
- Licence holder qualifications
- Responsibilities and obligations of Authorized Representatives
- Sole Authorized Representative requirements
- Manufacturing site inspection requirements
- Free Sale Certificate (FSC) requirements
- Quality Management System (QMS) requirements
- Product testing requirements
- Clinical investigation requirements
- Clinical evaluation requirements
- Post-market surveillance obligations
- Certificate validity periods
- Licence renewal procedures and fees
- Licence variation procedures and fees
- Certificate formats
- Licence transfer feasibility, procedures, and associated costs
- Interpretation of newly issued regulations and compliance strategies
- And many other regulatory topics
If you have any questions regarding global medical device registration or regulatory compliance, GRZAN Group Limited is always ready to assist. Our regulatory specialists provide one-on-one professional consultation and tailor-made market access solutions to help you navigate international regulatory requirements with confidence.
Although the exhibition has come to an end, our collaboration and communication continue.
We sincerely thank every customer, partner, and industry colleague who visited our booth. We look forward to staying connected, building lasting partnerships, and working together to create new opportunities in the global medical device market.