1. The first operating enterprise should provide the following information (1) Pharmaceutical manufacturer 1. Copies of the "Business License" and "Drug Production License" stamped with the original seal of the manufacturer 2. Copies of the stamped manufacturer Relevant certificates of the company's quality certification such as the GMP certification certificate with the original seal 3. A copy of the trademark registration certificate with the original seal of the production company 4. A power of attorney from the legal person with the original seal of the production company and the signature of the company's legal representative, and indicating the authorization Authorization scope and validity period 5. Copy of the salesperson’s ID card 6. Quality assurance agreement or quality commitment letter 7. Certificate of honor obtained by the enterprise in terms of quality, etc. (2) Pharmaceutical operating enterprise 1. Business license stamped with the original seal of the operating enterprise " and a copy of the "Pharmaceutical Business License" 2. GSP certification certificate with the original seal of the operating enterprise and other relevant certificates of the enterprise's quality certification 3. Legal person's power of attorney stamped with the original seal of the operating enterprise and signed by the legal representative of the enterprise, and Indicate the scope and validity period of the entrustment. 4. Copy of the salesperson’s ID card. 5. Quality assurance agreement or quality commitment letter. 6. Certificate of honor obtained in terms of industry quality, etc. 2. The following information should be provided for the first varieties: (Incoming goods from the production enterprise) 1. A copy of the production approval number stamped with the original seal of the manufacturing enterprise 2. A copy of the drug quality standards (national standards) stamped with the original seal of the manufacturing enterprise 3. A qualified drug inspection report stamped with the original seal of the manufacturing enterprise or its quality agency Copy of the book (single) 4. For the first business variety of the trade name, relevant supporting documents stamped with the original seal of the production unit should be provided. If the trade name is registered as a trademark, a copy of the corresponding trademark registration certificate should also be provided. 5. Stamping A copy of the price approval document with the original seal of the manufacturer 6. For drugs that are new drugs or protected varieties of traditional Chinese medicine, copies of the new drug certificate and protected variety certificate of traditional Chinese medicine with the original seal of the manufacturer should be provided 7. Drug packaging with the original seal of the manufacturer , Approval documents and actual samples of labels and instructions 8. Provide physical samples of drugs