The process of obtaining a periosteal stripping NMPA domestic registration certificate may vary depending on the specific product nature and requirements, but usually includes the following general steps:
Preparation phase: Learn more about the regulations, standards, and technical documentation for periosteal ionization before starting the process. Ensure that the product complies with the regulations of the NMPA.
Application Preparation: Collect and prepare all necessary documents and information, including application**, product technical documents, quality management system documents, production processes, etc.
Submit an application: Submit the completed application materials to the NMPA or its designee. Make sure that the application** is filled out correctly and that all documents meet the requirements.
Preliminary Examination: The NMPA will conduct a preliminary review of the application to ensure that all necessary documents and information have been provided and that the relevant regulations and standards are complied with.
Technical Evaluation: Conduct technical evaluation of products, including laboratory tests, clinical trials, etc., to ensure the quality, safety, and effectiveness of products.
GMP checks: GMP checks are carried out by the manufacturer to ensure that the production process meets the relevant standards.
Professional Review: The relevant professional review committee will review the application materials, including technical documents, clinical data, etc., and make recommendations.
Publicity: Publicize eligible products and solicit public opinions.
Approval and Certification: NMPA will finalize the application and issue a domestic registration certificate.