Second, the preparation of the declaration document, download and fill out the "Medical Device Network Sales Information Form".
Third, with the "supervision and management of the sale of medical devices network approach" required by the relevant materials to the local provincial drug supervision and management department for the record.
Fourth, by the drug regulatory department on-site verification of materials, in line with the provisions of the record to be issued to the medical device network trading third-party platform for the record voucher, the submission of information is incomplete or does not meet the statutory circumstances, should be a one-time notification of the need to supplement the material matters.
Fifth, the third-party platform providers need to accept the provincial drug regulatory authorities within three months after the filing of an on-site inspection.
Through the third-party platform for online sales of medical devices enterprises, need to cooperate with the third-party platform for the production and operation of medical equipment license or filing certificates, medical device registration certificate or filing certificates, business license and other materials for review.