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YY/T 0576-2024 English PDF

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Q: Should I purchase the latest version YY/T 0576-2024?

Yes. Unless special scenarios such as technical constraints or academic study, you should always prioritize to purchase the latest version YY/T 0576-2024 even if the enforcement date is in future. Complying with the latest version means that, by default, it also complies with all the earlier versions, technically.

US$199.00 · In stock
Delivery: <= 3 days. True-PDF full-copy in English will be manually translated and delivered via email.
YY/T 0576-2024: Columbia blood agar medium
Status: Valid

YY/T 0576: Historical versions

Standard ID	USD	BUY PDF	Lead-Days	Standard Title (Description)	Status
YY/T 0576-2024	199	Add to Cart	3 days	Columbia blood agar medium	Valid
YY/T 0576-2005	219	Add to Cart	3 days	Columbia blood agar base medium	Valid

Similar standards

YY/T 0653 YY/T 0588 YY/T 0589 YY/T 0688.2 YY/T 0655

Basic data

Standard ID: YY/T 0576-2024 (YY/T0576-2024)
Description (Translated English): Columbia blood agar medium
Sector / Industry: Medical Device & Pharmaceutical Industry Standard (Recommended)
Classification of Chinese Standard: C44
Classification of International Standard: 11.100.10
Word Count Estimation: 10,161
Date of Issue: 2024-09-29
Date of Implementation: 2025-10-15
Older Standard (superseded by this standard): YY/T 0576-2005
Issuing agency(ies): State Drug Administration
Summary: This standard specifies the main components and preparation methods, requirements, labels and instructions for use, packaging, transportation and storage of Columbia blood agar culture medium, and specifies the corresponding test methods. This standard applies to Columbia blood agar culture medium, including dry powder culture medium and plate culture medium.

YY/T 0576-2024: Columbia blood agar medium

---This is a DRAFT version for illustration, not a final translation. Full copy of true-PDF in English version (including equations, symbols, images, flow-chart, tables, and figures etc.) will be manually/carefully translated upon your order.
ICS 11.100.10 CCSC44 Pharmaceutical Industry Standards of the People's Republic of China Replaces YY/T 0576-2005 Columbia blood agar Released on 2024-09-29 Implementation on October 15, 2025 The State Drug Administration issued

Foreword

This document is in accordance with the provisions of GB/T 1.1-2020 "Guidelines for standardization work Part 1.Structure and drafting rules for standardization documents" Drafting. This document replaces YY/T 0576-2005 Columbia Blood Agar Medium. Compared with YY/T 0576-2005, except for the structural adjustment In addition to editorial changes, the main technical changes are as follows. --- Changed the scope of the standard (see Chapter 1, Chapter 1 of the.2005 edition); --- Changed the "culture medium" in the terms and definitions (see Chapter 3, Chapter 3 of the.2005 edition); --- Added "4.2 Preparation Method" (see Chapter 4); ---Changed "loss on drying" to "water content", added appearance, thickness, pH, microbial limit and growth in "plate culture medium" The performance index requirements of the test have been expanded to include the “stability” performance index requirements (see Chapter 5, Chapter 5 of the.2005 edition); --- The test method has been changed (see Chapter 6, Chapter 6 of the.2005 edition); --- Deleted "Instructions for Use" (see Chapter 7 of the.2005 edition); --- Changed the signs and labels (see Chapter 7, Chapter 8 of the.2005 edition); --- Changed packaging, transportation and storage (see Chapter 8, Chapter 9 of the.2005 edition); --- Columbia blood agar growth test (see Appendix A, Appendix A of the.2005 edition) has been changed. Please note that some of the contents of this document may involve patents. The issuing organization of this document does not assume the responsibility for identifying patents. This document is proposed by the State Food and Drug Administration. This document is under the jurisdiction of the National Technical Committee for Standardization of Medical Clinical Testing Laboratories and In Vitro Diagnostic Systems (SAC/TC136). This document was drafted by. China Food and Drug Inspection Institute, Henan Provincial Drug and Medical Device Inspection Institute (Henan Provincial Vaccine Approval Center), Shanghai Institute of Medical Device Inspection, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Zhengzhou Antu Bioengineering Co., Ltd., Zhengzhou Bo Sai Biotechnology Co., Ltd., Zhongxiu Technology Co., Ltd., Qingdao High-tech Industrial Park Haibo Biotechnology Co., Ltd., Beijing San Pharmaceutical Technology Co., Ltd. The main drafters of this document are. Yu Ting, Li Fengchun, Deng Min, Yi Qiaolian, Yang Yongkang, Ding Kunfeng, Tan Weili, Cai Xiangrong, Wang Jinheng, Bao Xueyin, Zhang Caiyu, Qu Shoufang, Sun Nan, Hu Zebin, Jia Zheng, Zhang Juanli, Li Guilin, and Zhang Xiaoguo. The previous versions of this document and the documents it replaces are as follows. ---First published in.2005 as YY/T 0576-2005; ---This is the first revision. Columbia blood agar

1 Scope

This document specifies the main components and preparation, requirements, identification, labeling and instructions for use, packaging, transportation, etc. of Columbia blood agar medium. and storage, and describes the corresponding test methods. This document applies to Columbia blood agar culture medium, including dry powder culture medium and plate culture medium.

2 Normative references

The contents of the following documents constitute the essential clauses of this document through normative references in this document. For referenced documents without a date, only the version corresponding to that date applies to this document; for referenced documents without a date, the latest version (including all amendments) applies to This document. GB/T 191 Pictorial markings for packaging, storage and transportation GB/T 29791.2 Information provided by the manufacturer of in vitro diagnostic medical devices (labeling) Part 2.Professional in vitro diagnostic reagents JJF1070-2023 Rules for the measurement and inspection of the net content of quantitatively packaged goods Pharmacopoeia of the People's Republic of China

3 Terms and definitions

The following terms and definitions apply to this document. 3.1 culture medium Prepared by artificial methods, containing natural and/or synthetic ingredients, for the cultivation, separation, identification, research and preservation of microorganisms Liquid, semi-solid or solid mixed nutrient products. 3.2 Quality control strain quality control strain Microorganisms used for quality control and performance testing of culture media. 3.3 colony forming unit; CFU In the counting of live bacteria culture, the colonies formed by the growth and reproduction of a single bacterium or multiple bacterium clusters on a solid culture medium are called It expresses the number of viable bacteria. 4 Main ingredients and preparation method (applicable to dry powder culture medium) 4.1 Main ingredients Trypticase or tryptone 10.0g Beef heart powder 3.0g Corn starch 1.0g Peptone 5.0g ......

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Tips & Frequently Asked Questions:

Question 1: How long will the true-PDF of YY/T 0576-2024_English be delivered?

Answer: Upon your order, we will start to translate YY/T 0576-2024_English as soon as possible, and keep you informed of the progress. The lead time is typically 1 ~ 3 working days. The lengthier the document the longer the lead time.

Question 2: Can I share the purchased PDF of YY/T 0576-2024_English with my colleagues?

Answer: Yes. The purchased PDF of YY/T 0576-2024_English will be deemed to be sold to your employer/organization who actually pays for it, including your colleagues and your employer's intranet.

Question 3: Does the price include tax/VAT?

Answer: Yes. Our tax invoice, downloaded/delivered in 9 seconds, includes all tax/VAT and complies with 100+ countries' tax regulations (tax exempted in 100+ countries) -- See Avoidance of Double Taxation Agreements (DTAs): List of DTAs signed between Singapore and 100+ countries

Question 4: Do you accept my currency other than USD?

Answer: Yes. If you need your currency to be printed on the invoice, please write an email to Sales@ChineseStandard.net. In 2 working-hours, we will create a special link for you to pay in any currencies. Otherwise, follow the normal steps: Add to Cart -- Checkout -- Select your currency to pay.

Question 5: Should I purchase the latest version YY/T 0576-2024?

Answer: Yes. Unless special scenarios such as technical constraints or academic study, you should always prioritize to purchase the latest version YY/T 0576-2024 even if the enforcement date is in future. Complying with the latest version means that, by default, it also complies with all the earlier versions, technically.