enow.com Web Search

  1. Ads

    related to: legal label guidelines for lotions medical equipment

Search results

  1. Results from the WOW.Com Content Network
  2. Single use medical device reprocessing - Wikipedia

    en.wikipedia.org/wiki/Single_Use_Medical_Device...

    The practice of reusing medical devices labeled for only one use began in hospitals in the late 1970s. [8] After a thorough review by the U.S. FDA in 1999 and 2000, [8] the agency released a guidance document for reprocessed SUDs that began regulating the sale of these reprocessed devices on the market, [9] under the condition that third-party reprocessors would be treated as the manufacturer ...

  3. Global Harmonization Task Force - Wikipedia

    en.wikipedia.org/wiki/Global_Harmonization_Task...

    The Global Harmonization Task Force (GHTF) was “a voluntary group of representatives from national medical device regulatory authorities (such as the U.S. Food and Drug Administration (FDA)) and the members of the medical device industry” [1] whose goal was the standardization of medical device regulation across the world.

  4. ISO 13485 - Wikipedia

    en.wikipedia.org/wiki/ISO_13485

    ISO 13485 Medical devices -- Quality management systems -- Requirements for regulatory purposes is a voluntary standard, [1] published by International Organization for Standardization (ISO) for the first time in 1996, and contains a comprehensive quality management system for the design and manufacture of medical devices.

  5. Single-use medical devices - Wikipedia

    en.wikipedia.org/wiki/Single-use_medical_devices

    Single-use medical devices include any medical equipment, instrument or apparatus having the ability to only be used once in a hospital or clinic and then disposed. The Food and Drug Administration defines this as any device entitled by its manufacturer that it is intended use is for one single patient and one procedure only. [ 1 ]

  6. Community Guidelines - AOL Legal

    legal.aol.com/legacy/community_guidelines/index.html

    We offer a diverse and robust community through a wide range of products, Services, and online areas (such as chat rooms and message boards). Some products, Services, or areas may carry additional standards. Please review and abide by the standards of the areas you frequent. The account holder is responsible for all activities on that account.

  7. Drugs and Cosmetics Rules, 1945 - Wikipedia

    en.wikipedia.org/wiki/Drugs_and_Cosmetics_Rules...

    "Drugs and Cosmetics Rules, 1945" (PDF). Central Drugs Standard Control Organization.Archived from the original (PDF) on 31 October 2005.; A Review on the Current Classification and Regulatory Provisions for Medicines in Drug & Cosmetic Act, in the light of Present Day Context Recommendations for Drugs & Cosmetics Rules with context of Drug Schedules

  1. Ads

    related to: legal label guidelines for lotions medical equipment