Chapter I General Provisions Article 1 These Regulations are hereby formulated with a view to strengthening the supervision and administration of medical devices, ensuring their safety and effectiveness and protecting human health and life safety.

1.The Direction for the Application Form for Registration 1) All the contents shall be in both Chinese and English； 2) All the contents must be printed；

China Food and Drug Administration (CFDA) recently released the 2014 Drug Review Annual Report. The Annual Report describes the general situation of drug registration acceptance,