When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  2. Collaborative practice agreement - Wikipedia

    en.wikipedia.org/wiki/Collaborative_practice...

    Regulations for CPAs in Connecticut are defined by the Connecticut General Statutes and Regulations, Title 20, Sections 20-631-1 through 20-631-3. [32] A PharmD degree is sufficient qualifications for engaging in CPAs in Connecticut, though other criteria are also available for Bachelor of Science in Pharmacy pharmacists with less than 10 years ...

  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. Pharmacy Competition and Consumer Choice Act of 2011

    en.wikipedia.org/wiki/Pharmacy_Competition_and...

    The Pharmacy Competition and Consumer Choice Act of 2011 (H.R. 1971) is the legislation that was introduced in the 112th United States Congress on May 24, 2011, with the full title of the bill stating to "amend the Public Health Service Act to ensure transparency and proper operation of pharmacy benefit managers". [1]

  5. Drug Quality and Security Act - Wikipedia

    en.wikipedia.org/wiki/Drug_Quality_and_Security_Act

    Signed into law by President Barack Obama on November 27, 2013 The Drug Quality and Security Act ( H.R. 3204 ) is a law that amended the Federal Food, Drug, and Cosmetic Act to grant the Food and Drug Administration more authority to regulate and monitor the manufacturing of compounded drugs. [ 1 ]

  6. Title 21 of the Code of Federal Regulations - Wikipedia

    en.wikipedia.org/wiki/Title_21_of_the_Code_of...

    Title 21 is the portion of the Code of Federal Regulations that governs food and drugs within the United States for the Food and Drug Administration (FDA), the Drug Enforcement Administration (DEA), and the Office of National Drug Control Policy (ONDCP). [1] It is divided into three chapters: Chapter I — Food and Drug Administration

  7. Federal Food, Drug, and Cosmetic Act of 1938 - Wikipedia

    en.wikipedia.org/wiki/Federal_Food,_Drug,_and...

    The United States Federal Food, Drug, and Cosmetic Act (abbreviated as FFDCA, FDCA, or FD&C) is a set of laws passed by the United States Congress in 1938 giving authority to the U.S. Food and Drug Administration (FDA) to oversee the safety of food, drugs, medical devices, and cosmetics.

  8. American Society for Pharmacy Law - Wikipedia

    en.wikipedia.org/wiki/American_Society_for...

    ASPL is a nonprofit organization with the purposes of furthering knowledge in the law related to pharmacists, pharmacies, the provision of pharmaceutical care, the manufacturing and distribution of drugs, and other food, drug, and medical device policy issues; communicating accurate legal educational information; and providing educational ...

  9. Pharmacist-to-pharmacy technician ratio - Wikipedia

    en.wikipedia.org/wiki/Pharmacist-to-pharmacy...

    The pharmacist-to-pharmacy technician ratio is a legal regulation that establishes the maximum number of pharmacy technicians that may be supervised by a licensed pharmacist at one given time. For example, a pharmacist-to-pharmacy technician ratio of 1:3 would mean that three people are allowed to be working as pharmacy technicians at one time ...