On the afternoon of January 12th, the "Medical Device CDMO" salon hosted by the Shenzhen Medical Device Quality Management Promotion Association was successfully held in Shenzhen. The project leader of MeHow Medical's MAH project was invited as a special guest to share insights on "Medical Device Registration Holder Outsourcing Production".

The project leader of MeHow Medical's MAH project elaborated on the regulatory requirements for outsourcing production, the responsibilities between the registration holder and the contracted party, and the practical management of production under the registration holder system.

During the presentation, Mr. Fu emphasized, "Obtaining registration approval is not the end, but the beginning of continuous supervision! Both the registration holder and the contracted party need self-discipline, accountability for the product, continuous learning, and effective supervision after the product is launched."

With the promulgation of the "Medical Device Supervision and Management Regulations" (State Council Decree No. 739), and the comprehensive implementation of the MAH system, CDMO (Contract Development and Manufacturing Organization) has become a trend in the medical device industry. 

Through the sharing and exchange at this salon, the Shenzhen Medical Device Quality Promotion Association and participating enterprises fully recognized the achievements of MeHow Medical in a new project development, production management, and quality system construction.

As the first manufacturing enterprise in Guangdong Province to participate in the pilot program, MeHow Medical has successfully undertaken and completed multiple products under the Marketing Authorization Holder system for Class II and Class III medical devices. In the next step, MeHow Medical will continue to enhance its quality management level, consolidate its core competitiveness with outstanding innovation capabilities and high-quality product quality, and undertake more projects from registration holders!