Hello:
　　As we execute the new version, manufacturers providing raw materials, auxiliary materials, packaging materials and equipment to our company shall provide the following four parts of materials (They are used for filing. Thank you for your cooperation! Manufacturers with incomplete materials cannot be selected as partners.)
　　Part I:
　　1. Enterprise profile
　　2. Quality assurance agreement
　　3. Quality management organization chart
　　4. Salesman ID card
　　5. Salesman employment certificate
　　6. Quality standards
　　7. Quality inspection report
　　8. Business license
　　9. Legal person authorization
　　10. Drug production licence
　　11. Drug registration certificate
　　12. Organization chart
　　13. Drug GMP certification
　　14. Laboratory equipment list
　　15. Production workshop equipment list
　　16. Supplier Survey List. We will provide you with an electronic version and you shall print it out. The document is attached to the compressed file, and each page shall be stamped with a fresh red seal after completion.
　　Part II:
　　F-SOP0130002-07 Supplier On-site Audit Record (The electronic version is attached, and you shall print it out. Each page shall be stamped with a fresh red seal after completion).
　　The above paper materials shall be provided in triplicate (each page shall be stamped with a fresh red seal!) and then sent by express, thank you!!
　　Part III:
　　Supplier Notice (it shall be signed and stamped and then mailed together with the above materials)
　　Please send to the following address(by express of YTO, ZTO, YUNDA, SF, STO, TTK and HTKY):
　　Panjin Hengchanglong Pharmaceutical Co., Ltd., Dawa District, Panjin City, Liaoning Province. Xu Qiang Tel.: 18242759028