Reference product refers to the standard substance used for identification, inspection, content determination and calibration of the performance of the verification instrument, the use of chemical methods to determine, that is, the general instrument is called the reference product. There should be a special person responsible for the management of the reference products, and be familiar with the nature and storage conditions of the reference products, and establish receipt records. What are the identification and storage requirements for reference products? The following is a small edition of Bolinda to introduce you.

Identification requirements for reference products:

1. Outsourced or homemade work reference products should have clear identification and instructions.

2, for the self-made reference products, the label must have the name, batch number, preparation date, purity, expiration date and storage conditions, etc., for some special reference products, the reference products are also required to indicate the quantity, safety guidelines and handling guidelines and other information.

3, the identification content of the reference product, the identification content should at least include the name of the reference product, batch number, expiration date, preparation date, content or titer, first opening date and storage conditions.

Storage requirements for reference products:

1. Air conditioning facilities should be set up in the storage room to ensure that the room is dry, cool, ventilated and shielded from light, and special varieties should be properly stored in strict accordance with the stipulated storage conditions.

2. The reference product after opening should be stored in the dryer. Outside each dryer, there should be a special code for the reference number to show the storage location.

The above content is the introduction of the identification and storage requirements of the reference product, the reference product and the standard product refers to the national drug standards for identification, inspection, content determination, impurities and related substances inspection and other standard substances, it is an integral part of the national drug standards.