List of medicines reimbursed by health insurance

When editing the list of medicines reimbursed by health insurance, I will follow the following steps:

1. Gathering information: Understand the relevant laws and regulations and health insurance policies, as well as the requirements and standards of the health insurance department for reimbursement of medicines. At the same time, communicate with the health insurance department and relevant professionals to obtain the latest drug catalog list.

2. Review drug information: Carefully review the relevant information of each drug, including the name, specification, manufacturer, indications, contraindications, and dosage of the drug. Ensure the accuracy and completeness of drug information.

3. Categorization: According to the nature and use of drugs, drugs are categorized and organized, for example, according to pharmacological effects, therapeutic areas, routes of administration and so on. This makes it easier for users to find and use.

4. Updating the list: According to the requirements of the medical insurance department and the provisions of regular updates, the list of drug catalogs is updated in a timely manner. Delete drugs that are no longer applicable, add newly listed drugs, and revise and update the information of existing drugs.

5. Checking and proofreading: After the editing is completed, checking and proofreading work is carried out to ensure that the drug information in the list is accurate and to avoid any errors and omissions.

6. Publishing and publicizing: Publish the edited list of medicines reimbursed by health insurance to appropriate platforms, such as the official website of the health insurance department and the internal system of the medical institutions. At the same time, through appropriate publicity and promotion, users will be able to understand and correctly use the Medicare reimbursement drug catalog list.

Legal basis:

Law of the People's Republic of China*** and the State of China on Drug Administration (Revised in 2019):

Chapter 1 General Provisions Article 7 In engaging in the activities of drug development, production, operation, and use, it shall comply with the laws, rules and regulations, rules and regulations, standards, and norms, and shall ensure that the information of the whole process is true, accurate, complete, and traceable.