-
Categories
-
Pharmaceutical Intermediates
-
Active Pharmaceutical Ingredients
-
Food Additives
- Industrial Coatings
- Agrochemicals
- Dyes and Pigments
- Surfactant
- Flavors and Fragrances
- Chemical Reagents
- Catalyst and Auxiliary
- Natural Products
- Inorganic Chemistry
-
Organic Chemistry
-
Biochemical Engineering
- Analytical Chemistry
- Cosmetic Ingredient
-
Pharmaceutical Intermediates
Promotion
ECHEMI Mall
Wholesale
Weekly Price
Exhibition
News
-
Trade Service
In recent years, the Chinese medicine industry is showing a relatively fast pace of development, industry analysis, its industrialization of large-scale development or can drive the whole industrial chain of Chinese medicine standardization, standardized development.
, it is worth noting that while the Chinese medicine industry is accelerating development, the quality of Chinese medicine is also getting more and more attention, especially Chinese medicine tablets.
recently, the State Drug Administration issued the "Notice on 25 batches of drugs do not meet the requirements" (No. 55 of 2020) shows that a total of 25 batches of drugs were found to be unqualified, of which 7 batches are Chinese medicine tablets.
, non-compliance items involving characteristics, identification, content determination, total ash, etc.
analysis of the reasons behind its repeated exposure to non-conformity, the industry believes that this is mainly due to the quality of Chinese medicine tablets easily affected by the mode of production and management.
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 beyond reprocess.
background, the development of the beverage tablet industry and even the whole Chinese medicine industry urgently need to strengthen the supervision and management of enterprises.
industry believes that in order to ensure the quality and safety of Chinese medicine tablets, the establishment of quality traceability system is essential.
the supervision of Chinese medicine tablets should emphasize the standardization, applicability and scientific nature of management on the basis of the existing law of the development of Chinese medicine.
However, the supervision of Chinese medicine tablets must involve upstream and downstream industries, which requires concerted efforts by all parties to form a co-push mechanism to promote the establishment and strengthening of the management mode of the whole industrial chain of Chinese medicine by strengthening the management of Chinese medicine tablets.
, especially the promotion of drug regulatory authorities and national policies, can promote the healthy development of the industry.
fact, in recent years the state 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;
The author believes that from these requirements, it can be inferred that the medical institution's Chinese medicine tablets traceability system should have to provide consumers with inquiries to trace their consumption of Chinese medicine tablets source details and for regulators to provide inquiries trace Chinese medicine tablets detailed where to go.
As of August 26, 2019, Article 32 of the newly amended Drug Administration Law also clearly states that drug market license holders, pharmaceutical manufacturers, pharmaceutical manufacturers and medical institutions shall establish and implement a drug quality traceability system to ensure drug traceability.
august 27, the State Drug Administration issued three information standards, such as the Basic Technical Requirements for Drug Trace Systems, and said they would be implemented from the date of publication.
basic technology of drug traceability system requires that drug traceability system should have the function of providing drug traceability information query to consumers and providing trace data query function to regulators.
From a series of comprehensive policy documents, the state is constantly establishing and perfecting the quality traceability mechanism of Chinese medicine, and many medical institutions that dare to innovate and have social responsibility have also begun to incorporate the construction of the traceability system of Chinese medicine tablets into the key work.
In line with this trend, the industry 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 can be traced, to traceable, 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 demonstration and promotion, and at the same time promote the further development of the Chinese medicine industry.