1. GMP registration consultation is the embodiment of total quality management in the pharmaceutical industry& lt; Regulations for the Implementation of the Standardization Law of the People's Republic of China& gt; Article 18 stipulates that "standards and industrial standards are divided into mandatory standards and recommendatory standards". Drug standards are mandatory.

2、產(chǎn)品質(zhì)量咨詢(xún)的種類(lèi)按質(zhì)量咨詢(xún)的責(zé)任不同，可分為自我咨詢(xún)、使用方咨詢(xún)、第三方咨詢(xún)。按咨詢(xún)內(nèi)容不同，可分為質(zhì)量咨詢(xún)、體系咨詢(xún)、安全咨詢(xún)。藥品關(guān)系人命安危，因此藥品咨詢(xún)屬于安全咨詢(xún)，是屬于一種強(qiáng)制性的咨詢(xún)。

2. The types of product quality consultation can be divided into self consultation, user consultation and third-party consultation according to the different responsibilities of quality consultation. According to different consultation contents, it can be divided into quality consultation, system consultation and safety consultation. Drugs are related to the safety of human life, so drug consultation is a kind of safety consultation and a kind of mandatory consultation.

3、GMP是一部體現(xiàn)質(zhì)量管理和質(zhì)量保證新概念的國(guó)際GMP，其特點(diǎn)體現(xiàn)在它是結(jié)合iso9000~9004標(biāo)準(zhǔn)系列修改而成的標(biāo)準(zhǔn)。而在國(guó)外有些執(zhí)行著美國(guó)FDA咨詢(xún)的標(biāo)準(zhǔn)，我國(guó)也有些單位通過(guò)了美國(guó)FDA咨詢(xún)。

3. GMP is an international GMP that embodies the new concept of quality management and quality assurance, and its characteristics are embodied in that it is a modified standard combined with iso9000~9004 standard series. While in foreign countries, some units implement the standards of FDA consultation in the United States, and in China, some units have passed the FDA consultation in the United States.

4、國(guó)際咨詢(xún)的意義本身就是不僅要加強(qiáng)藥廠內(nèi)部諸多質(zhì)量因素的過(guò)程控制，也要對(duì)藥廠外部關(guān)鍵質(zhì)量因素有所控制。如配方、原料、輔料、包裝材料、儀器設(shè)備以及建筑材料的質(zhì)量采取控制措施。

4. The significance of international consultation is not only to strengthen the process control of many quality factors inside the pharmaceutical factory, but also to control the key quality factors outside the pharmaceutical factory. Take control measures for the quality of formula, raw materials, auxiliary materials, packaging materials, instruments and equipment and building materials.

5、藥品監(jiān)督管理局是代表對(duì)藥品獨(dú)立地進(jìn)行第三方公正評(píng)價(jià)的GMP咨詢(xún)機(jī)構(gòu)，其代碼C12。負(fù)責(zé)國(guó)際藥品貿(mào)易中優(yōu)先采購(gòu)、使用推薦、優(yōu)先受理新藥藥品申請(qǐng)。迄至1998年6月31日末取得咨詢(xún)的企業(yè)，藥品監(jiān)督管理部門(mén)將不再受理新藥生產(chǎn)的申請(qǐng)。

5. The Drug Administration is a GMP consulting agency that independently conducts a third-party fair evaluation of drugs, its code is C12. Be responsible for giving priority to purchase, use and recommendation, and receiving new drug applications in international drug trade. For enterprises that have obtained consultation by the end of June 31, 1998, the drug regulatory authorities will no longer accept applications for new drug production.

6、GMP注冊(cè)咨詢(xún)是集軟件、硬件、安全、衛(wèi)生、環(huán)保于一身的強(qiáng)制性咨詢(xún)，那么它就必須建立和運(yùn)行著科學(xué)的、公認(rèn)的國(guó)際管理體系，要請(qǐng)有資歷的第二方(咨詢(xún)機(jī)構(gòu))匯同本企業(yè)專(zhuān)家進(jìn)行整體策劃、評(píng)估，制訂出適合本企業(yè)(含國(guó)際標(biāo)準(zhǔn)、標(biāo)準(zhǔn)、行業(yè)標(biāo)準(zhǔn))規(guī)范的質(zhì)量管理手冊(cè)及作業(yè)指導(dǎo)書(shū)，在學(xué)習(xí)、培訓(xùn)、運(yùn)轉(zhuǎn)的不斷修正過(guò)程中，再來(lái)申請(qǐng)GMP咨詢(xún)才是每個(gè)藥業(yè)人明智的選擇。

6. GMP registration consultation is a mandatory consultation integrating software, hardware, safety, health and environmental protection. Therefore, it must establish and operate a scientific and recognized international management system. A qualified second party (consulting agency) should be invited to participate in the overall planning and evaluation together with the enterprise's experts, so as to develop a quality management manual and operation instructions suitable for the enterprise's (including international standards, standards and industrial standards) specifications In the process of continuous correction of operation, it is a wise choice for every pharmaceutical company to apply for GMP consultation again.

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