Tyre Capsule was declared unqualified due to loss of drying weight

Recently, Jilin Jichun Pharmaceutical Co., Ltd. was again exposed to the black list. According to an announcement from the Zhejiang Food and Drug Administration, in the third quarter of 2011, the Bureau completed 1118 batches of sample tests for pharmaceutical products in Zhejiang Province, and 1,113 batches passed inspections, and 5 batches of unqualified medicines, with a passing rate of 99.6%. Among them, a fetal treasure capsule produced by Jilin Jichun Pharmaceutical Co., Ltd. failed due to loss of drying weight.

Jichun Pharmaceutical has been criticized by the Food and Drug Administration for the third consecutive year. According to statistics, as early as 2010, Jichun Pharmaceutical had been unsuccessfully named by the Zhejiang Provincial Food and Drug Administration: the name of the drug was fetal treasure capsule, the production unit was Jilin Jichun Pharmaceutical Co., Ltd., the batch number was 080402, and the specification was 0.3g. A year later, the Zhejiang Food and Drug Administration again issued a quality announcement that a fetal treasure capsule produced by Jichun Pharmaceutical did not meet the requirements of the relevant standards, and the unqualified item was loss on drying.

The same as in 2010 and 2011, the data released by the Zhejiang Food and Drug Administration in recent days showed that the tire capsules produced by the company were once again found to be unqualified: Loss on drying, 8.6% (not to exceed 7.0%). To this end, the reporter called and transmitted the newsletter yesterday to Ji Chun Pharmaceutical's external media promotion to Mr. Zhao. However, to the reporter's deadline, Mr. Zhao did not give any response to the newspaper. The quality and safety of medicines undoubtedly affect everyone's sensitive nerves. The reporter learned that the State Council Legislative Affairs Office has recently announced the "Policy Management Quality Management (Revised Draft)" to solicit opinions from the society. The reporter noted that in addition to the refinement of some of the contents, the specifications also added some new regulations such as “drug recalls”. The draft clarified that companies engaged in the wholesale and retail of pharmaceuticals should set up quality management departments responsible for the collection and management of quality information, the identification of substandard drugs, and the supervision of the handling of substandard drugs.

Glossary:

Loss on drying refers to the weight of a drug lost after drying to constant weight under the specified conditions, usually expressed as a percentage

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