X00 标准化、质量管理 标准查询与下载

EN ISO 6886:2016 动植物油脂氧化稳定性的测定(加速氧化试验)(ISO 6886:2016)

Diese Internationale Norm legt ein Verfahren zur Bestimmung der Oxidationsstabilität von Fetten und Ölen unter extremen Bedingungen fest, die eine schnelle Oxidation bewirken: hohe Temperatur und starker Luftstrom. Das Verfahren ermöglicht nicht die Bestimmung der Stabilität von Fetten und Ölen bei Umgebungstemperaturen, es lässt jedoch einen Vergleich der Wirksamkeit von den Fetten und Ölen zugesetzten Antioxidantien zu. Das Verfahren ist sowohl auf native als auch auf raffinierte tierische und pflanzliche Fette und Öle anwendbar. Milch und Milcherzeugnisse (oder Fett aus Milch und Milcherzeugnissen) sind vom Anwendungsbereich dieser Internationalen Norm ausgenommen. ANMERKUNG Das Vorliegen von flüchtigen Fettsäuren und flüchtigen sauren Oxidationsprodukten verhindert eine genaue Messung.

Animal and vegetable fats and oils - Determination of oxidative stability (accelerated oxidation test)

NY/T 896-2015 绿色食品 产品抽样准则

本标准规定了绿色食品样品抽取的术语和定义、一般要求、抽样程序和抽样方法。 本标准适用于绿色食品产品的样品抽取。

Green food.Guideline on product sampling

CFR 21-14.100-2015 食品和药物. 第14部分:在公开咨询委员会之前的公开听证会. 第F子部分:标准咨询委员会. 第14.100节:标准咨询委员会的名单.

Standing advisory committees and the dates of their establishment are as follows:

Food and drugs. Part14:Public hearing before a public advisory committee. SubpartF:Standing advisory committees. Section14.100:List of standing advisory committees.

CFR 21-1301.29-2014 食品和药物. 第1301部分:控制物质的注册制造商,分销商和药剂师. 第1301.29节:登记弃权;为了个人授权免除从业者登记,通过美国核管理委员会或者国家医生的同意,使用执照或者许可证,并管理DaTscanTM药物产品.

(a) The requirement of registration is waived for persons administering the drug product DaTscanTM to a patient for diagnostic purposes if the person is authorized by a valid medical use license or permit issued by the United States Nuclear Regulatory Commission (NRC) or NRC master materials licensee or an agreement state authorizing the person to receive, possess, use, or transfer byproduct material in accordance with NRC or agreement state rules and regulations.

Food and drugs. Part1301:Registration of manufacturers, distributors, and dispensers of controlled substances. Section1301.29:Registration waivers; exemption from practitioner registration for persons authorized by a United States Nuclear Regulatory Commi

CFR 21-21.43-2014 食品和药物. 第21部分:隐私保护. 第D子部分:隐私法记录系统中访问记录的通知程序. 第21.40节:访问请求的记录.

(a) Access may be granted to requested records by: (1) Mailing a copy of the records to the requesting individual, or

Food and drugs. Part21:Protection of privacy. SubpartD—Procedures for Notification of and Access to Records in Privacy Act Record Systems. Section21.43:Access to requested records.

CFR 21-21.52-2014 食品和药物. 第21部分:隐私保护. 第E子部分:程序纪录的修改请求. 第21.52节:拒绝修改记录的行政上诉.

(a) If an individual disagrees with a refusal under §21.51(a)(2) to amend a record, he or she may appeal that refusal to the Commissioner of Food and Drugs,(see the address on the agency’s web site at http://www.fda.gov).

Food and drugs. Part21:Protection of privacy. SubpartE:Procedures for requests for amendment of records. Section21.52:Administrative appeals of refusals to amend records.

CFR 21-10.85-2014 食品和药物. 第10部分:管理实践和过程. 第B子部分:一般行政程序. 第10.85节:咨询意见.

(a) An interested person may request an advisory opinion from the Commissioner on a matter of general applicability.

Food and drugs. Part10:Administrative practices and procedures. SubpartB:General administrative procedures. Section10.85:Advisory opinions.

CFR 21-20.3-2014 食品和药物. 第20部分:公共信息. 第A子部分:官员的证词和信息. 第20.3节:食品和药物管理局的记录的认证和鉴定.

(a) Upon request, the Food and Drug administration will certify the authenticity of copies of records that are requested to be disclosed pursuant to this Part or will authenticate copies of records previously disclosed.

Food and drugs. Part20:Public information. SubpartA:Official testimony and information. Section20.3:Certification and authentication of Food and Drug Administration records.

CFR 21-20.26-2014 食品和药物. 第20部分:公共信息. 第B子部分:总方针. 第20.26节:某些记录的索引.

(a) Indexes shall be maintained, and revised at least quarterly, for the following Food and Drug Administration records:

Food and drugs. Part20:Public information. SubpartB:General policy. Section20.26:Indexes of certain records.

CFR 21-20.30-2014 食品和药物. 第20部分:公共信息. 第B子部分:总方针. 第20.30节:食品和药物管理局员工的信息的自由.

(a) The office responsible for Agency compliance with the Freedom of Information Act and this Part is the Division of Freedom of Informationat the address located on the agency’s web site at http://www.fda.gov.

Food and drugs. Part20:Public information. SubpartB:General policy. Section20.30:Food and Drug Administration freedom of information staff.

CFR 21-20.40-2014 食品和药物. 第20部分:公共信息. 第C子部分:程序和费用. 第20.40节:纪录归档的请求.

(a) All requests for Food and Drug Administration records shall be made in writing by mailing or delivering the request to the Freedom of Information Staff at the address on the agency’s web site at http://www.fda.gov or by faxing it to the fax number listed on the agency’s web site at http:// www.fda.gov. All requests must contain the postal address and telephone number of the requester and the name of the person responsible for payment of any fees that may be charged.

Food and drugs. Part20:Public information. SubpartC:Procedures and Fees. Section20.40:Filing a request for records.

CFR 21-20.107-2014 食品和药物. 第20部分:公共信息. 第F子部分:特定类别的可用性记录. 第20.107节:食品和药物管理局手册.

(a) Food and Drug Administration administrative staff manuals and instructions that affect a member of the public are available for public disclosure. An index of all such manuals is available by writing to the Division of Freedom of Informationat the address

Food and drugs. Part20:Public information. SubpartF:Availability of specific categories of records. Section20.107:Food and Drug Administration manuals.

CFR 21-20.120-2014 食品和药物. 第20部分:公共信息. 第F子部分:特定类别的可用性记录. 第20.120节:记录可在食品和药物管理局公共阅览室得到.

(a) The Freedom of Information Staff and the Division of Dockets Manage ment Public Reading Room are located at the same address. Both are located n rm. 1061, 5630 Fishers Lane, Rock ville, MD 20852. The telephone number or the Division of Docket Management s 301–827–6860; the telephone number or the Freedom of Information Staff’s Public Reading Room is located at the

Food and drugs. Part20:Public information. SubpartF:Availability of specific categories of records. Section20.120:Records available in Food and Drug Administration Public Reading Rooms.

CFR 21-21.32-2014 食品和药物. 第20部分:公共信息. 第F子部分:特定类别记录的要求. 第21.32节:人事纪录.

(a) Present and former Food and Drug Administration employees desiring access to personnel records about themselves should consult system notices applicable to the agency’s personnel records that are published by the Office of Personnel Management and the Department as well as any notice issued by the Food and Drug Administration.

Food and drugs. Part21:Protection of privacy. SubpartC:Requirements for specific categories of records. Section21.32:Personnel records.

CFR 21-21.40-2014 食品和药物. 第21部分:隐私保护. 第D子部分:隐私法记录系统中访问记录的通知程序. 第21.40节:通知和访问的程序提交请求.

(a) An individual may request that the Food and Drug Administration notify him whether a Privacy Act Record System contains records about him that are retrieved by reference to his name or other personal identifier. An individual may at the same time, or after receiving notification that such a record about him exists, requests that he be given access to the record.

Food and drugs. Part21:Protection of privacy. SubpartD—Procedures for Notification of and Access to Records in Privacy Act Record Systems. Section21.40 Procedures for submitting requests for notification and access.

CFR 21-5.1110-2014 食品和药物. 第5部分:组织. 第M子部分:组织. 第5.1110节:美国食品药品管理局公共信息办事处.

(a) Division of Dockets Management. The Division of Dockets Management public room is located in rm. 1061, 5630 Fishers Lane, Rockville, MD 20852, Telephone: 301–827–6860.

Food and drugs. Part5:Organization. SubpartM:Organization. Section5.1110:FDA public information offices.

CFR 21-10.90-2014 食品和药物. 第10部分:管理实践和过程. 第B子部分:一般行政程序. 第10.90节:食品药品监督管理局规定,建议,和协议.

(a) Regulations. FDA regulations are issued in the FEDERAL REGISTER under §10.40 or §10.50 and codified in the Code of Federal Regulations. Regulations may contain provisions that will be enforced as legal requirements, or which are intended only as guidance documents and recommendations, or both. The dissemination of draft notices and regulations is subject to §10.80.

Food and drugs. Part10:Administrative practices and procedures. SubpartB:General administrative procedures. Section10.90:Food and Drug Administration regulations, recommendations, and agreements.

CFR 21-10.95-2014 食品和药物. 第10部分:管理实践和过程. 第B子部分:一般行政程序. 第10.95节:标准制定外活动的参与.

(a) General. This section applies to part icipation by FDA employees in standard-setting activities outside the agency. Standard-setting activities include matters such as the development of performance characteristics, testing methodology, manufacturing practices, product standards, scientific protocols, compliance criteria, ingredient specifications, labeling, or other technical or policy criteria. FDA encourages employee participation in outside standard-setting activities that are in the public interest.

Food and drugs. Part10:Administrative practices and procedures. SubpartB:General administrative procedures. Section10.95:Participation in outside standard-setting activities.

CFR 21-14.65-2014 食品和药物. 第14部分:在公开咨询委员会之前的公开听证会. 第D子部分:会议和听证会之前咨询委员会的记录. 第14.65节:公众调查和咨询委员会的请求记录.

(a) Public inquiries on general committee matters, except requests for vrecords, are to be directed to the Committee Management Officer in the Advisory Committee Oversight and Management Staff, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 32, Rm. 5103, Silver Spring, MD 20993.

Food and drugs. Part14:Public hearing before a public advisory committee. SubpartD:Records of meetings and hearings before advisory committees. Section14.65:Public inquiries and requests for advisory committee records.

CFR 21-21.41-2014 食品和药物. 第21部分:隐私保护. 第D子部分:隐私法记录系统中访问记录的通知程序. 第21.40节:请求的处理.

(a) An individual or his guardian under §21.75 shall not be required to show any justification or need to obtain notification under §21.42 or access to a record under §21.43.

Food and drugs. Part21:Protection of privacy. SubpartD—Procedures for Notification of and Access to Records in Privacy Act Record Systems. Section21.41:Processing of requests.