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  2. Pharmaceutical policy - Wikipedia

    en.wikipedia.org/wiki/Pharmaceutical_policy

    While patent laws are written to apply to all inventions, whether mechanical, pharmaceutical, or electronic, the interpretations of patent law made by government patent granting agencies (the United States Patent and Trademark Office, for example) and courts, can be very subject-matter specific with significant impact on the incentives for drug development and the availability of lower-priced ...

  3. Prescription Drug Marketing Act - Wikipedia

    en.wikipedia.org/wiki/Prescription_Drug...

    The Prescription Drug Marketing Act (PDMA) of 1987 (P.L. 100-293, 102 Stat. 95) is a law of the United States federal government.It establishes legal safeguards for prescription drug distribution to ensure safe and effective pharmaceuticals and is designed to discourage the sale of counterfeit, adulterated, misbranded, sub potent, and expired prescription drugs.

  4. Federal drug policy of the United States - Wikipedia

    en.wikipedia.org/wiki/Federal_drug_policy_of_the...

    The drug policy in the United States is the activity of the federal government relating to the regulation of drugs. Starting in the early 1900s, the United States government began enforcing drug policies. These policies criminalized drugs such as opium, morphine, heroin, and cocaine outside of medical use.

  5. Comprehensive Drug Abuse Prevention and Control Act of 1970

    en.wikipedia.org/wiki/Comprehensive_Drug_Abuse...

    The Comprehensive Drug Abuse Prevention and Control Act of 1970, Pub. L. 91–513, 84 Stat. 1236, enacted October 27, 1970, is a United States federal law that, with subsequent modifications, requires the pharmaceutical industry to maintain physical security and strict record keeping for certain types of drugs. [1]

  6. 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 ...

  7. Pharmaceutical industry - Wikipedia

    en.wikipedia.org/wiki/Pharmaceutical_industry

    The United States had still by far the most valued pharmaceutical industry with 40% of global valuation. [ 78 ] 2023 was a year of layoffs for at least 10,000 people across 129 public biotech firms globally, albeit most small firms; this was a significant increase in reductions versus 2022 was in part due to worsening global financial ...

  8. Tariffs, federal government spending cuts restrain US ... - AOL

    www.aol.com/news/tariffs-federal-government...

    U.S. business activity nearly stalled in February amid mounting fears over tariffs on imports and deep cuts in federal government spending, erasing all the gains notched in the aftermath of ...

  9. Category : Pharmaceutical regulation in the United States

    en.wikipedia.org/wiki/Category:Pharmaceutical...

    This page was last edited on 28 December 2022, at 01:53 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.