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  2. Clinical Laboratory Improvement Amendments - Wikipedia

    en.wikipedia.org/wiki/Clinical_Laboratory...

    The Clinical Laboratory Improvement Amendments (CLIA) of 1988 are United States federal regulatory standards that apply to all clinical laboratory testing performed on humans in the United States, except clinical trials and basic research.

  3. Significant New Alternatives Policy - Wikipedia

    en.wikipedia.org/wiki/Significant_New...

    Unacceptable in new equipment, except as otherwise allowed under a narrowed use limit, as of January 1, 2024. Acceptable: HFC-245fa Unacceptable in new equipment, except as otherwise allowed under a narrowed use limit, as of January 1, 2024. Acceptable: Acceptable: Acceptable: HFE-347mcc3 (heptafluoropropyl methyl ether) Acceptable: Acceptable

  4. EPA tightens limits on a chemical used to sterilize medical ...

    www.aol.com/news/epa-tightens-limits-chemical...

    The EPA’s generally acceptable increase in lifetime cancer risk is 1 in 10,000. Ethylene oxide is a gas used to sterilize roughly half of all medical devices and is also used to ensure the ...

  5. Clinical and Laboratory Standards Institute - Wikipedia

    en.wikipedia.org/wiki/Clinical_and_Laboratory...

    The Clinical and Laboratory Standards Institute (CLSI) is a volunteer-driven, membership-supported, not-for-profit, standards development organization. CLSI promotes the development and use of voluntary laboratory consensus standards and guidelines within the health care community.

  6. Tolerable daily intake - Wikipedia

    en.wikipedia.org/wiki/Tolerable_daily_intake

    The threshold limit value (TLV) of a chemical substance is a level to which it is believed a worker can be exposed day after day for a working lifetime without adverse effects. Examples of Tolerable Daily Intake

  7. List of stringent regulatory authorities - Wikipedia

    en.wikipedia.org/wiki/List_of_stringent...

    A stringent regulatory authority is a regulatory authority which is: a) a member of the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH), being the European Commission, the US Food and Drug Administration and the Ministry of Health, Labour and Welfare of Japan also represented by the Pharmaceuticals and Medical Devices Agency (as before ...

  8. Medicare Part D catastrophic coverage: What to know - AOL

    www.aol.com/medicare-part-d-catastrophic...

    For 2024, the OOP limit is $8,000 out of pocket. A person will then be out of the coverage gap for Medicare prescription drug coverage and will automatically get catastrophic coverage.

  9. Medical laboratory - Wikipedia

    en.wikipedia.org/wiki/Medical_laboratory

    Credibility of medical laboratories is paramount to the health and safety of the patients relying on the testing services provided by these labs. Credentialing agencies vary by country. The international standard in use today for the accreditation of medical laboratories is ISO 15189 - Medical laboratories - Requirements for quality and competence.