[double day celebration] the "Encyclopedia" of medicine circle is free!

In the era of big data, the retrieval and utilization of medical information has become one of the professional skills that people in the circle must master For a drug circle deep like the sea, how to step from "small white" counter attack to become a big guy, from then on "see all the mountains and small"? As the old saying goes: if a worker wants to do good things, he must first sharpen his tools If a tool wants to do his best, he must first obtain his method From September 21 to September 28, yaozhi.com launched 8 treasure books of common databases in the pharmaceutical industry to help you step up to the top Through customs clearance, we must see the "drug registration and acceptance database" of [Baodian I], "global drug R & D database" of [Baodian III], "clinical trial database" of [Baodian iv], "generic drug consistency evaluation database" of [Baodian v], "bid winning database" of [Baodian vi], "drug sales database" Today, Xiaozhi's seventh winning classic is Yaozhi's "China drug standard database" [Baodian 7] brief introduction of "China drug standard database" of Yaozhi 01 Baodian the "China drug standard database" of Yaozhi basically contains all the national drug quality standard information, totaling more than 40000 pieces, and the vast majority of standards are available for free inquiry and download Up to now, the information contained in the database is as follows: 02 the strategy of the treasure book: 1 retrieval conditions: the search field of the China medicine standard database includes the name of drug, standard source and text query Among them, the database supports the fuzzy search of "drug name", that is, it only needs to enter the corresponding keywords in the "drug name" search box, such as "vitamin" or "C tablet" can be queried Standard source can select standard types, and different standard types will display different file contents Retrieval results: Taking "Tianma headache tablet" as an example, four corresponding "standard sources" and documents are displayed after retrieval The information can be viewed or downloaded for free! Other related databases: those directly related to "Chinese drug standard database" of Yaozhi are the "Chinese drug standard database" of Yaozhi, which is also the "drug standard database" marked by the arrow in the figure above The database contains all the information of national and local quality standards for medicinal materials, totaling more than 20000 pieces, and the vast majority of standards provide full-text query and download The specific standards are as follows: the retrieval interface of "medicinal materials standard database" of Yaozhi "03 the secret collection of" the Chinese medicine standard database "of Yaozhi is a free and open database, and the information collected is from the official documents It is called the "Encyclopedia" of the pharmaceutical industry All the information of the national drug quality standards can be found in this database Therefore, in order to make good use of this "Encyclopedia", Xiaozhi has several key words about drug standards Please accept them! Pharmaceutical standards refer to the technical regulations made by the state on the quality specifications and inspection methods of pharmaceuticals, which are the legal basis for the production, circulation, use, inspection and supervision of pharmaceuticals 2 The connotation of drug quality includes three aspects: authenticity, purity and quality The concentrated expression of the three is the effectiveness and safety in use 3 Drug inspection report: the report issued by the drug factory or drug inspection agency after inspection according to drug standards 4 Auxiliary materials: refers to the general designation of all pharmaceutical materials in the prescription except for the main drug, which are added to solve the problem of the formulation's formability, effectiveness, stability and safety In addition to shaping, acting as carrier and improving stability, pharmaceutical excipients also have important functions such as solubilization, solubilization, slow and controlled release, which may affect the safety and effectiveness of drugs 5 Drug registration standard: refers to the standard approved by the national drug administration to the applicant for specific drugs, which mainly includes the production process / quality inspection procedures, quality indicators, inspection methods and other technical requirements Drugs that have been approved for marketing must be produced in accordance with the approved registration standards 6 Infrared spectrum (IR): the infrared spectrum is that molecules can selectively absorb some wavelengths of infrared rays, which causes the transition of vibration and rotation energy levels in molecules The infrared absorption spectrum of substances can be obtained by detecting the absorption of infrared rays, also known as molecular vibration spectrum or vibration rotation spectrum It is generally used for qualitative analysis and requires reference materials 7 Chromatogram: chromatogram refers to the image of the detection signal of the separated component over time The signal time curve obtained by the sample flowing through the chromatographic column and detector is also called the chromatographic outflow curve 8 Traditional Chinese medicine: a kind of Medicine Guided by the theory of traditional Chinese medicine to collect, process, prepare, explain the mechanism of action, and guide the clinical application 9 Chinese medicinal materials: Chinese medicinal materials refer to the original medicinal materials used under the guidance of traditional Chinese medicine for the treatment of diseases 10 Chinese patent medicine: Chinese patent medicine is a kind of commercialized traditional Chinese medicine preparation approved by the State Drug Administration, which is made of Chinese herbal medicine as raw materials, under the guidance of the theory of traditional Chinese medicine and in order to prevent and treat diseases, and processed into a certain dosage form according to the prescribed prescription and preparation process 11 Chinese Herbal Pieces: Chinese herbal pieces can be directly used in the clinical practice of traditional Chinese medicine after being processed according to the theory and method of traditional Chinese medicine This concept shows that there is no absolute boundary between Chinese herbal medicine and Chinese herbal pieces Chinese herbal pieces include some slices of Chinese herbal medicine processed in the production area, original pieces of Chinese herbal medicine and pieces cut and processed The first two kinds of management should be regarded as Chinese herbal medicine, only according to the theory of Chinese medicine in the formula, preparation for the pieces of understanding 12 Prescription of traditional Chinese medicine: the Chinese side of prescription refers to medical prescription, prescription, and prescription Prescription is the prescription for treating diseases 13 Medical instruments: medical instruments refer to instruments, equipment, instruments, in vitro diagnostic reagents, calibrators, materials and other similar or related articles directly or indirectly used for human body, including required computer software 14 Classification of medical devices: the State implements classified management of medical devices according to the degree of risk The first is the low risk level, the implementation of conventional management can ensure its safety and effective medical devices (it shall be examined and approved by the drug regulatory department of the people's Government of a city divided into districts, and a product production registration certificate shall be issued.) The second type is a kind of medical device with moderate risk, which needs strict control and management to ensure its safety and effectiveness (the drug regulatory department of the people's Government of a province, autonomous region or municipality directly under the central government shall examine and approve the application and issue a product production registration certificate.) The third type is a kind of medical device with high risk, which needs to take special measures to strictly control and manage to ensure its safety and effectiveness (the production of class III medical devices shall be examined and approved by the drug regulatory department under the State Council, and a production registration certificate shall be issued The production of class II and class III medical devices shall be subject to clinical verification.) Questions you may encounter? 1 What are the domestic drug registration standards? Domestic registration Standard No.: ybh2013010 Standard No.: WS1 - (x-095) - 2011z import registration standard (Note: import standard is not foreign standard) Standard No.: jx2013010 2 Does the registration standard implemented by the enterprise must be higher than the pharmacopoeia standard? The standards implemented by the enterprise shall be non-public standards, and the registration standards shall not be lower than the Pharmacopoeia standards 3 What are the commonly used foreign Pharmacopoeia standards? At present, the foreign Pharmacopoeia with high frequency of use by enterprises (included in the "foreign Pharmacopoeia online database" of pharmaceutical Intelligence) include: usp32; usp36; usp37; bp2009; bp2010; bp2013, bp2013; jp16 (Japanese version, English version); ep7.0, 7.5, 8.0; Pharmacopoeia of India 2010 Edition; finally, Xiaozhi warm tips: Strategy in hand, gift you have! Xiaozhi's big data dictionary presented to you during the Mid Autumn Festival will play an important and important role in the National Day "big data World War I, award winning" activity (secretly tell you that some of the contents of the dictionary will be made into a small interesting answer bank)! Answer points will affect your prize! Pay attention, pay attention! Statement: this opinion only represents the author, not the position of yaozhi.com, welcome to exchange and supplement in the message area; if you need to reprint, please be sure to indicate the author and source of the article.