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YY/T 1244-2014 PDF in English


YY/T 1244-2014 (YY/T1244-2014, YYT 1244-2014, YYT1244-2014)
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YY/T 1244-2014: PDF in English (YYT 1244-2014)

YY/T 1244-2014 YY ICS 11.100 C 44 Pharmaceutical Industry Standard of the People’s Republic of China Purified water for in vitro diagnostic reagents ISSUED ON. JUNE 17, 2014 IMPLEMENTED ON. JULY 1, 2015 Issued by. State Food and Drug Administration Table of Contents Foreword ... 3  1 Scope ... 4  2 Normative references ... 4  3 Terms and definitions ... 4  4 Requirements ... 4  5 Test methods ... 5  References ... 7  Foreword This Standard was drafted according to the rules given by GB/T 1.1-2009. Please note that some contents of this Document may involve patents. The issuing authority of this document does not undertake the responsibility for the identification of these patents. This Standard was proposed by State Food and Drug Administration. This Standard shall be under the jurisdiction of the Standardization Technical Committee of National Medical Clinical Test Laboratory and in Vitro Diagnostic System (SAC/TC 136). Main drafting organizations of this Standard. Beijing Institute of Medical Device Testing, Beckman Coulter Experimental System (Suzhou) Co., Ltd., BIOSINO Biotechnology Co., Ltd., Zhongshan University Da’an Gene Co., Ltd., and National Institutes for Food and Drug Control. Main drafters of this Standard. Bi Chunlei, Chen Xingbao, Wang Jianqing, Gao Xunian, and Huang Jie. Purified water for in vitro diagnostic reagents 1 Scope  This Standard specifies terms and definitions, requirements, and test methods of purified water in-vitro diagnostic reagents. Purified water for in-vitro diagnostic reagents can be used for in-vitro diagnostic reagents’ production, general reagent preparation in medical laboratory, instrument and equipment cleaning etc. If there are special requirements for reagents production, REFER to the relevant standards or FORMULATE a special requirement (such as the special requirements for particle by blood cell counting reagents; the special requirements for DNA enzymes, RNA enzymes, and protease by molecular biology reagents). 2 Normative references  The provisions in following documents become the provisions of this Standard through reference in this Standard. For dated references, the subsequent amendments (excluding corrections) or revisions do not apply to this Standard. Pharmacopoeia of the People's Republic of China 2010 Edition (Volume II) 3 Terms and definitions  The following terms and definitions apply to this document. 3.1 purified water This product is the water obtained from drinking water by distillation method, ion-exchange method, reverse-osmosis method or other suitable methods, without any additives. 4 Requirements  4.1 Characters This product shall be clear and colorless liquid. References [1] GB/T 6682-2008 Water for analytical laboratory use - Specification and test methods [2] National Pharmacopoeia Committee. Pharmacopoeia of the People's Republic of China 2010 Edition (Volume II) [3] CLSI (C3-A4 2006). Preparation and test of water for clinical laboratory reagents Approved guideline. 4th Edition. [4] ISO 3696.1987 Water for analytical laboratory use - Specification and test methods ......
 
Source: Above contents are excerpted from the PDF -- translated/reviewed by: www.chinesestandard.net / Wayne Zheng et al.