As required by Regulations for the Supervision and Administration of Medical Devices,Measures for the Examination of Advertisements for Medical Devices,if an advertisement published through a certain medium or form contains such contents as the name of the medical device, the scope of application of the product, its performance structure and composition, and its mechanism of action, it shall apply for the approval number of the advertisement for the medical device.
Any advertisement for medical devices published without examination and approval,or any advertisement for medical devices published is inconsistent with the content of the approval，shall be punished by the advertising supervision and administration authorities in accordance with the Advertising Law,where the act constitutes false advertising or false publicity, the advertising supervision and administration authorities shall punish it in accordance with the Advertising Law or the Law of the People's Republic of China Against Unfair Competition.
C.Documents provided by client
1.The applicant's subject qualification certificate.
2.The document that the holder of the product registration certificate or filing credential authorizes the operating enterprise as the applicant.
3.Product registration certificate/filing credential, product standard/technical requirements.
4.Production license or business license of the applicant.
5.Labels and manuals of the product to be registered or filed.
6.Trademark registration, patent, copyright certificate and other certificates.
D.Professional Services from ZOOP
To provide professional services fro pre-checking advertising content,and to apply for advertising approval number to the NMPA on behalf.
Estimated processing period for advertising examination and approval : 2 months