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    Home > Active Ingredient News > Drugs Articles > A batch of unqualified drugs were suspended and recalled, and Chinese medicine tablets accounted for the majority

    A batch of unqualified drugs were suspended and recalled, and Chinese medicine tablets accounted for the majority

    • Last Update: 2020-11-15
    • Source: Internet
    • Author: User
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    "Pharmaceutical Network Industry Dynamics" September 21, Heilongjiang Province Drug Administration issued a drug quality sampling announcement.
    According to the Bulletin, the eight batches found in the sampling did not meet the requirements of the drug, of which 7 were Chinese medicine tablets: hot licorice, hot mutton (drink tablets), golden cherry blossoms, vinegar cream, fried pecans, hemp nuts, hawthorn;
    it is worth mentioning that this non-conforming items are mostly "symptoms", there are also a number of varieties of insect decay phenomenon.
    fact, Chinese medicine tablets sampling non-conformity has been common in the industry.
    this year, a large number of Chinese medicine tablets have been reported to stop selling, recall.
    Such as April 9, Shandong Provincial Drug Administration issued the 2020 Issue 1 drug quality sampling notice, showing that a total of 16 batches of drugs do not meet the standards, of which 13 batches of Chinese medicine tablets.
    involved in the varieties include white-headed, big-headed, wearing heart lotus, bone skin, semi-summer and so on.
    It is worth noting, however, that combined with the drug regulatory department's annual flight inspection report, it can be clearly found that the reasons for the non-conformity of chinese medicine tablets are mostly related to "the nature".
    so why is this? What exactly is "nature"? It is understood that the characteristic identification of Chinese medicine drink tablets refers to the traditional experience identification, is the use of human senses, that is, eye, taste, nose, ear, hand touch and so on to identify Chinese medicine tablets, the main content includes shape, specifications, size, surface or cut color, characteristics, texture, break phenomenon, odor, water test, fire test.
    because of historical reasons, the identification of sexuality in China's Chinese medicine tablets supervision has been the main way to determine whether Chinese medicine tablets qualified or not.
    " is not qualified, which means that the product will be disqualified from circulation in the market.
    " In general, Chinese medicine is the foundation of Chinese medicine clinical and traditional Chinese medicine industry, is the foundation of the foundation, we must establish strict, scientific, reasonable and applicable standards, and the nature is to judge the quality of Chinese medicine is an important identification standard.
    for Chinese medicine tablets because of the nature of repeatedly exposed unqualified, the industry believes that this is mainly the quality of Chinese medicine drink tablets are vulnerable to the production mode and management mode of the impact.
    traditional, backward production mode and unscientific management concepts have caused the instability of the quality of Chinese medicine tablets.
    addition, coupled with the disorderly competition in the market, poor quality products mixed with fish and dragon, to fake the truth, drinking tablets are questioned is also undeniable.
    , in this context, the development of the beverage tablet industry and even the whole Chinese medicine industry, it is urgent to strengthen the supervision and management of enterprises.
    fact, in recent years, the country has begun to slowly establish a quality traceability system for Chinese herbal medicines.
    As early as 2007, the State Administration of Traditional Chinese Medicine and the Ministry of Health issued the "Hospital Chinese Medicine Tablets Management Code" on the requirements: Chinese medicine tablets procurement and acceptance of the source of Chinese medicine tablets need to be registered one by one;
    August 26, 2019, Article 32 of the newly amended Drug Administration Law also clearly states that drug market license holders, pharmaceutical manufacturers, pharmaceutical operators and medical institutions shall establish and implement a drug quality traceability system to ensure drug traceability.
    , the State Drug Administration also issued three information standards, such as "Basic Technical Requirements for Drug Trace Systems".
    from a series of policy documents, the state is constantly establishing and improving the quality of Chinese medicine traceability mechanism.
    According to this trend, the industry generally believes that in the future, including Traditional Chinese medicine, Chinese medicine tablets, Traditional Chinese medicine, including the whole process of drug traceability system will be accelerated to build, to achieve the source of traceability, traceability, the public independent inspection, and gradually form the whole industry chain of Chinese medicine quality traceability, for the Chinese medicine industry traceability system to play a good role in promoting the further development of the Chinese medicine industry.
    In addition, industry experts also suggest that as soon as possible to establish a large number of Chinese medicine, commonly used Chinese medicine futures market, Chinese herbal medicine, drink tablets for real-time supply, storage, estimated amount, usage statistics.
    , related enterprises should also increase investment to improve the professional and technical personnel capacity of Chinese medicine tablets, as well as the upgrading of testing equipment.
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