1, the drug license, staff qualifications, health certificates.
2, staff files: (staff file registration form, staff personal training registration form, staff personal health file, staff health summary table)
3, drug information files: (document quality information circulation card, drug quality inquiries quality complaint registration questionnaire, customer opinion book, drug quality file registration form, drug quality information analysis summary table, quality management system check and (
4, the supply unit and the first drug files: (supply unit file form and related information, the first enterprise approval form, the first varieties of approval form, the first varieties of quality file registration form)
5, drug purchase files: (purchase of drugs schedule, drug purchase inspection and approval of the registration form).
6, instrumentation files: (Instrumentation list, instrumentation inspection and maintenance records, strong testing instruments calibration record sheet).
7, drug maintenance files: (temperature and humidity record sheet, key maintenance varieties to determine the table and maintenance files, drug maintenance inspection records, Chinese herbal medicines, Chinese medicine tablets maintenance records, Chinese herbal medicines, Chinese medicine tablets, loading bucket registration and review records). The
8, the drug sales registration file: (split drug registration form, prescription drug sales registration record form, Chinese herbal medicines and Chinese medicine tablets transfer sales registration record form).
9, unqualified drugs file: (near-expiry drugs and slow-moving drug statements, unqualified drug confirmation form and investigation and processing form, unqualified drug registration ledger, unqualified drug destruction registration approval form).
The above is over the GSP to prepare the information.
The above is the information to be prepared for GSP.