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Wysłany: Wto 23:52, 15 Mar 2011
Temat postu: Water and distilled water quality standards labora
,
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Laboratory Comparison of water and distilled water quality standards
Qualifying units should meet the requirements should comply with the provisions of 1. Above table shows three levels of water and distilled water for laboratory use in appearance, the same traits. 2. Three water restrictions H {value of 5.0 ~ 7.5 pH of distilled water using the term, according to methyl red and bromothymol blue color range of two indicators in the country we know the PH value of distilled water, 4.2 ~ 7.6 of the Q, should be said that = are almost ~ Ocean. 3. Test the limits of oxides that can be distilled water easily check oxides, plus three never provided 0.01tool / L potassium permanganate solution I. 0ml, boil 5 minutes the pale red should not completely faded, and distilled water,
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, provides spider O. 02mol / L potassium permanganate solution 0.1rnl,
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, boil for 10 minutes, pink may not completely disappear. That is, distilled water check the amount of potassium permanganate used in the water only three 1 / 5. And three levels of boiling water is still longer than long. Description of the inspection. Distilled water three requirements above. 4. Three water conductivity measurement, distilled water, although with this, but provides for chloride, sulfate and heavy metals such as calcium checks, both similar to both reflects the limits of electrolytes in water samples. 5. The presence of ammonia, although the kitchen can be reflected from the PH value of the individual as a single list, but it is not as good as distilled water standards the standard three point fine. 6. Carbon dioxide does volatile inspection, it is blue with the two-level water standards, discussion 1. A 92 levels from the GB6682_ water and 2. Though from the test project to see different, but the control of the ingredients are the same. 3. Overall, the Pharmacopoeia distilled water contained in the collection of its test items over GB6682 - 92 water projects in more than three and base, this may be because of distilled water amidine experiment, but also medicinal and park it. I believe that the community in a variety of quality products to provide notarial data measurement certification inspection agencies, the higher authorities should be specified whether the drug testing laboratory water? Or Pharmacopoeia Commission Pharmacopoeia in the preparation of the next version of whether the note back in Van out experiments with water must meet three sets of water in the GB6682-97 standard, the preparation of general preparation of water use distilled water, in distilled water in the body, can be distilled with the GB6682-92 in the third part of the same water, to a certain items according to GB6682 - 92 standard test water in three different projects listed separately. This easy-inspectors, and now the Archives of pharmaceutical development and utilization of information resources, Institute of Pharmaceutical Industry in Shandong Province, Shandong Qilu Pharmaceutical Factory Ma Mian Ying Wang, Institute of Ramie} j glanced case management development so far, from the last form of relief from the Treasury-style management to those who information development, consulting center direction. Development files for information on how resources contained in the file held as much as possible information resources quickly into productive forces, for the economic construction, became a hot topic of discussion file management is an important part of the development of archives which, in medicine here production development and utilization of archival information about that view. First, strengthen the collection of pharmaceutical production files. The pharmaceutical production technology development and utilization of pharmaceutical production file before the problem is to determine the file quality of the collection, utilization of high and low key. Pharmaceutical market has its particularity. Most products in the market demand curve showed a trend to lower the sales of a product, often asked to rebound after a period of time, due to poor ability to resist risks of SMEs frequently changing products, market trends favorable, and then resume production and this time, the production the use of technical information is particularly important. If the original records preserved, can avoid detours, improve efficiency, gain the initiative in the market, the original data is not complete,
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, you have to re-trial production, in particular,
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, more products such as labor-intensive processes, resources, problems sometimes arise and waste of time, resulting in economic losses. As the file manager has the responsibility to collect and preserve as complete as possible production technology of the original data. File management in the pharmaceutical production the State Pharmaceutical Administration of the Central Plains and the State Archives of medical records by category compiled a book on the pharmaceutical production files to develop a detailed classification. Classification is not difficult to learn well. The most important is to have a sense of responsibility and mission, to take the initiative to collect some data, draw conclusions, really play the role of medical records management. =, Computer and other modern equipment for the carrier. Business information provided funding of pharmaceutical thin file types with the efficiency of the development of today's knowledge economy era is the era of rapid development of information, file
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