Medical Industry Collections

Secure required certification by meeting performance and safety standards

Find the latest standards and European Union Directives for medical devices and products. The Medical Industry Collection provides a comprehensive collection of international regulatory material pertaining to device use and manufacturing. The EU Directives are a key component to attaining a CE Mark, necessary for products entering the EU. These medical industry technical specifications assure you can:

  • Ensure market share
  • Enhance product safety & effectiveness
  • Access consolidated standards research sources

Medical Industry Collections

Collection material comes from:
Association for the Advancement of Medical Instrumentation (AAMI)Canadian Standards Association (CSA)
ASTM International (ASTM)The Institute of Electrical and Electronics Engineers, Inc. (IEEE)
International Electrotechnical Commission (IEC)Association Connecting Electronics Industries (IPC)
International Organization for Standardization (ISO)Japanese Standards Association (JSA)
EU DirectivesNational Electrical Manufacturers Association (NEMA)
American Society of Mechanical Engineers (ASME)Society of Automotive Engineers (SAE)
American Society for Quality (ASQ)Underwriter's Laboratories, Inc. (UL)

Purchase Options

Full Online Standards SolutionIndividual Standards
Multiple standardsMinimal standards
Frequent purchases ($3000+/year)Infrequent purchases
Standards access or budget management, organization-wideLess than 5 employees use standards
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