ZH
RU
ES
listing
listing, Total:87 items.
In the international standard classification, listing involves: Finances. Banking. Monetary systems. Insurance, Mining equipment, Services, Medical equipment, Farming and forestry, Law. Administration, Quality, Company organization and management, Astronomy. Geodesy. Geography, Medical sciences and health care facilities in general, Pharmaceutics, Protection against crime, Agricultural machines, implements and equipment, Railway engineering in general, Installations in buildings, Construction technology, Transport, HEALTH CARE TECHNOLOGY, Wastes, (No title), Terminology (principles and coordination), Test conditions and procedures in general, Protection against fire.
US-FCR, listing
Professional Standard - Finance, listing
IX-EU/EC, listing
- MEDDEV 2.12-2-2004 GUIDELINES ON POST MARKET CLINICAL FOLLOW-UP
- 2014/C 337/03-2014 Summary of European Union decisions on marketing authorisations in respect of medicinal products
- (EC) NO 1093/97-1997 Commission Regulation Laying down Marketing Standards Applicable to Melons and Watermelons
- 88/627/EEC-1988 Council Directive on the Information to be Published When a Major Holding in a Listed Company is Acquired or Disposed of
- COM(87) 246-1987 Amended Proposal for a Council Directive Amending Directive 80/ 390/EEC Coordinating the Requirements for the Drawing up, Scrutiny and Distribution of the Listing Particulars to be Published for the Admission of Securities to Official Stock Exchange Listi
- NO 1176/2003-2003 COMMISSION REGULATION amending Regulation (EC) No 1019/2002 on marketing standards for olive oil
- 2007/C 144/06-2007 Summary of Community decisions on marketing authorizations in respect of medicinal products from 1 May 2007 to 31 May 2007
US-CFR-file, listing
- CFR 21-822.15-2013 Food and Drugs. Part822:Postmarket surveillance. Section822.15:How long must I conduct postmarket surveillance of my device?
- CFR 21-822.7-2013 Food and Drugs. Part822:Postmarket surveillance. Section822.7:What should I do if I do not agree that postmarket surveillance is appropriate?
- CFR 21-814.3-2014 Food and Drugs. Part814:Premarket approval of medical devices. Section814.3:Definitions.
- CFR 21-814.84-2013 Food and Drugs. Part814:Premarket approval of medical devices. Section814.84:Reports.
- CFR 21-814.20-2013 Food and Drugs. Part814:Premarket approval of medical devices. Section814.20:Application.
- CFR 21-814.39-2014 Food and Drugs. Part814:Premarket approval of medical devices. Section814.39:PMA supplements.
- CFR 21-814.100-2014 Food and Drugs. Part814:Premarket approval of medical devices. Section814.100:Purpose and scope.
- CFR 21-814.116-2014 Food and Drugs. Part814:Premarket approval of medical devices. Section814.116:Procedures for review of an HDE.
- CFR 21-814.44-2014 Food and Drugs. Part814:Premarket approval of medical devices. Section814.44:Procedures for review of a PMA.
- CFR 21-814.104-2014 Food and Drugs. Part814:Premarket approval of medical devices. Section814.104:Original applications.
- CFR 21-822.3-2013 Food and Drugs. Part822:Postmarket surveillance. Section822.3:How do you define the terms used in this part?
- CFR 21-822.9-2013 Food and Drugs. Part822:Postmarket surveillance. Section822.9:What must I include in my submission?
- CFR 21-73.530-2013 Food and Drugs. Part73:Listing of color additives exempt from certification. Section73.530:Spirulina extract.
- CFR 21-814.37-2014 Food and Drugs. Part814:Premarket approval of medical devices. Section814.37:PMA amendments and resubmitted PMAs.
- CFR 21-73.350-2013 Food and Drugs. Part73:Listing of color additives exempt from certification. Section73.350:Mica-based pearlescent pigments.
Korean Agency for Technology and Standards (KATS), listing
US-AAMI, listing
ES-UNE, listing
- UNE-CEN ISO/TR 20416:2020 Medical devices - Post-market surveillance for manufacturers (ISO/TR 20416:2020) (Endorsed by Asociación Española de Normalización in October of 2020.)
Group Standards of the People's Republic of China, listing
- T/CI 072-2022 ESG evaluation technical guideline for listed company
- T/CAGDE 220-2022 Guide to Legal Services for Mainland Enterprises Listing in Hong Kong
- T/SHSPTA 002-2023 Specification for entrusted distribution management by drug market authorization holders
- T/CCIIA 0003-2020 Guidelines for the ESG evaluation of listed companies in China's petroleum and chemical industry
- T/GDDL 3-2022 Compilation guide for land space ecological restoration planning of cities above prefecture level
- T/CACM 014-2016 Technical specification for hospital centralized monitoring of post-marketing safety of Chinese patent medicines
- T/CACM 1370.1-2021 Technical Specifications for the Revision of Safety Information in the Marketed Chinese Patent Medicine Instructions — General Principles
- T/CACM 1370.3-2021 Technical Specifications for the Revision of Safety Information in the Marketed Chinese Patent Medicine Instructions— Contraindications
- T/CNPPA 3019-2022 Guidance of equivalence/replaceability assessment and compatibility studies for postapproval changes to pharmaceutical packages
- T/CACM 1370.6-2021 Technical Specifications for the Revision of Safety Information in the Marketed Chinese Patent Medicine Instructions—Warnings
- T/CACM 1370.2-2021 Technical Specifications for the Revision of Safety Information in the Marketed Chinese Patent Medicine Instructions—Adverse Drug Reactions
- T/CACM 1370.4-2021 Technical Specifications for the Revision of Safety Information in the Marketed Chinese Patent Medicine Instructions—Precautions
- T/SHJX 002-2018 Code for Design of Shanghai Suburban Rail (Trial Implementation)
- T/CACM 1370.5-2021 Technical Specifications for the Revision of Safety Information in the Marketed Chinese Patent Medicine Instructions—Application for Specific Populations
- T/SHDSP 2-2023 Indicator System for Shanghai Data Merchant Evaluation
- T/SETA 0001-2019 Planning and selection of residential elevators in Shanghai
- T/SIIA 006-2022 Shanghai Quality Installation Engineering Award Evaluation Criteria
- T/SHJX 026-2021 Shanghai Inland River Port Standardized Technical Specifications
- T/SHBX 005-2021 Technical Specification for Reverse Logistics of Shanghai Wood Packaging
- T/SETA 0002-2019 Technical specification for elevator adding of existing residential buildings in Shanghai
- T/SRCA 000002-2018 Shanghai group standard group meal management service specification
- T/SMAFA 000036-2023 Shanghai digital orchard construction and evaluation standard
- T/SHJX 0017-2020 Code for Design of Shanghai Suburban Railway Vehicle Base
- T/SHJX 0016-2020 Specifications for Hydrogeological Survey of Railways in Shanghai Municipality (Trial)
- T/SHJX 0014-2020 Specifications for Geotechnical Engineering Survey of Shanghai Railway (Trial)
- T/SHQX 005-2023 Evaluation standard for Shanghai automobile quality Consumption Demonstration area
Association Francaise de Normalisation, listing
International Organization for Standardization (ISO), listing
British Standards Institution (BSI), listing
- PD CEN ISO/TR 20416:2020 Medical devices. Post-market surveillance for manufacturers
- 19/30401776 DC PD ISO/TR 20416. Medical devices. Post-market surveillance for manufacturers
- BS 6803-2:1986 Vehicle security alarm systems - Code of practice for systems installed after vehicle marketing
KR-KS, listing
Guizhou Provincial Standard of the People's Republic of China, listing
- DB5206/T 148-2022 Technical Regulations for Production of Heading Cabbage on the Market in Spring
CZ-CSN, listing
European Committee for Standardization (CEN), listing
Danish Standards Foundation, listing
American National Standards Institute （ANSI), listing
HU-MSZT, listing
RU-GOST R, listing
- GOST 31593-2012 Machines and equipment for wood industrial low landings. Safety requirements. Control methods
- GOST R 56701-2015 Medicines for medical applications. Guidance on nonclinical safety studies for the conduct of human clinical trials and marketing authorization for pharmaceuticals
Shanghai Provincial Standard of the People's Republic of China, listing
EU/EC - European Union/Commission Legislative Documents, listing
- 2009/C 146/03-2009 Summary of Community decisions on marketing authorizations in respect of medicinal products from 1 May 2009 to 31 May 2009 — Issuing of a marketing authorization (Article 13 of Regulation (EC) No 726/2004): Accepted (Published pursuant to Article 13 or Ar
- 2009/C 146/04-2009 Summary of Community decisions on marketing authorizations in respect of medicinal products from 1 May 2009 to 31 May 2009 — Issuing@ maintenance or modification of a national marketing authorisation (Decisions taken pursuant to Article 34 of Directive 20
Heilongjiang Provincial Standard of the People's Republic of China, listing
- DB23/T 3199-2022 Technical regulations for the construction and installation of above-ground municipal fire hydrants