echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Medical News > Latest Medical News > 13 batches were not tested.

    13 batches were not tested.

    • Last Update: 2020-10-20
    • Source: Internet
    • Author: User
    Search more information of high quality chemicals, good prices and reliable suppliers, visit www.echemi.com
    The notice shows that a total of 12 production enterprises (preparation units) marked a total of 11 varieties of 13 batches of drugs, after sampling does not meet the standard requirements, of which 10 varieties are Chinese medicine tablets: licorice, orange, yellow cypress, ginger half summer, lotus heart, former Hu, fist ginseng, meat tablets, mulberry parasitic, five plus skin.
    non-conforming items: content determination, moisture, traits, leaching, total ash, identification - microscopic characteristics The original text is as follows: In order to strengthen drug quality supervision, to ensure the safety of public drug use, according to the annual sampling work plan of the provincial drug regulatory bureau, the provincial bureau of drugs The production, operation and use units have carried out spot checks and inspections on the quality of medicines, and the situation of non-compliant drugs found in the spot checks is heeded as follows: First, after verification and confirmation, 11 varieties of 12 production enterprises (preparation units) marked a total of 13 batches of drugs, after sampling does not meet the standards.
    2. The relevant drug regulatory department has taken control measures such as seizure, seizure, suspension of sales and product recall of non-compliant products, and shall, in accordance with relevant laws and regulations, seriously investigate and punish the relevant production enterprises (preparation units) and sampled units in accordance with the law, and may inquire about the website of the relevant municipal market supervision authority.
    , for non-compliant products and corresponding production and operation enterprises and units, the relevant drug regulatory departments should strengthen supervision, urge them to identify the causes of the problems, formulate and implement corrective measures, and effectively eliminate hidden risks.
    he hedes this notice.
    Drug Administration, Shandong Province, September 17, 2020.
    This article is an English version of an article which is originally in the Chinese language on echemi.com and is provided for information purposes only. This website makes no representation or warranty of any kind, either expressed or implied, as to the accuracy, completeness ownership or reliability of the article or any translations thereof. If you have any concerns or complaints relating to the article, please send an email, providing a detailed description of the concern or complaint, to service@echemi.com. A staff member will contact you within 5 working days. Once verified, infringing content will be removed immediately.

    Related Articles

    Contact Us

    The source of this page with content of products and services is from Internet, which doesn't represent ECHEMI's opinion. If you have any queries, please write to service@echemi.com. It will be replied within 5 days.

    Moreover, if you find any instances of plagiarism from the page, please send email to service@echemi.com with relevant evidence.