2. Secondly, fill in the basic information of drugs in the form and fill in the quality inspection records of drugs according to the actual situation.
3. Then fill in the storage conditions of drugs, including storage temperature, humidity, lighting and other requirements. You can record the actual storage conditions and monitoring data in this section.
4, and then fill in the basic information of drug suppliers and manufacturers, including name, contact information, etc. , and record the information of suppliers and manufacturers for traceability and contact.
5. Finally, at the bottom or blank of the form, you can fill in the information or remarks that need to be recorded, which can include comments and suggestions on the quality of drugs.