The condition for applying for gcp certificate is that you can only apply for gcp certificate examination after attending gcp training. Choose to register at the Advanced Research Institute of China Food and Drug Administration; After the registration fee is confirmed successfully, gcp training will be conducted (the training will be in the form of video and audio, and you will be eligible for the exam after listening to the whole course).

The main responsibilities of gcp are:

(1) To be responsible for drafting the draft laws and regulations on the supervision and management of food (including food additives and health food, the same below), drugs (including traditional Chinese medicine and ethnic medicine, the same below), medical devices and cosmetics, and formulating policy plans.

Formulate departmental rules, promote the establishment of a mechanism to implement the main responsibility of food safety enterprises and the overall responsibility of local people's governments, establish a direct reporting system for major food and drug information, organize implementation, supervision and inspection, and focus on preventing regional and systematic food and drug safety risks.

(two) responsible for formulating measures for the implementation of food administrative licensing and supervising the implementation. Establish a mechanism for the investigation and management of food safety hazards, formulate the annual plan for national food safety inspection, and organize the implementation of major rectification and management programs.

Responsible for establishing a unified food safety information release system and releasing major food safety information. Participate in the formulation of food safety risk monitoring plan and food safety standards, and carry out food safety risk monitoring according to the food safety risk monitoring plan.

(three) responsible for organizing the formulation and publication of the national pharmacopoeia and other drugs and medical devices standards and classification management system, and supervise the implementation. Responsible for formulating quality management standards for research and development, production, operation and use of drugs and medical devices and supervising their implementation. Responsible for the registration, supervision and inspection of drugs and medical devices. Establish a monitoring system for adverse drug reactions and medical device adverse events, and carry out monitoring and disposal.

Formulate and improve the qualification access system for licensed pharmacists, and guide and supervise the registration of licensed pharmacists. Participate in the formulation of the national essential drug list and cooperate with the implementation of the national essential drug system. Formulate measures for the supervision and administration of cosmetics and supervise their implementation.