US FDA: Protecting Public Health & Safety - Essay Sample

Paper Type:  Essay
Pages:  3
Wordcount:  612 Words
Date:  2023-08-01
Categories: 

Introduction

Its principal function is to protect the general public health by ensuring the safety, security, and efficacy of veterinary and human drugs, medical devices, and biological products.

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The agency ensures that America’s food supply, products, and cosmetics are safe and do not emit radiations.

The agency also ensures the protection and conservation of public health by focusing on the excellence in health and safety of humanoid and veterinary drugs, injections, and other biomedical products and medical equipment.

Finally, the agency plays a significant role in the fight against America’s counterterrorism capability. It fulfills this mandate through its core duty of ensuring the security of the entire food being supplied. Secondly, fostering the development of all medical products, hence responding to any natural and deliberate evolving public health threats.

The Food and Drug Administration agency impacts the day to day operations of a pharmacist though the following. First, it through its legislative acts such as the Food, Drug, and Cosmetic Act of 1938 (Fain, Daubresse & Alexander, 2013). This law centers on food, medicine, and cosmetics. It impacts them directly since it restricts their practice in areas ranging from interstate commercial activities like misbranded and adulterated food and drinks and drugs (Fain, Daubresse & Alexander, 2013).

Another act that FDA has in store for the pharmacist is the 1970 Controlled substance Act (Fain, Daubresse & Alexander, 2013). This act directly impacts pharmacist practices since it demands that every pharmacist register, keep specific records and rules regarding the administration of controlled substances (Fain, Daubresse & Alexander, 2013).

FDA also requires all pharmacists to do record keeping. The agency gives guidelines that pharmacists should follow to maintain and keep proper medical records for at least a period exceeding two years (Fain, Daubresse & Alexander, 2013). These records have to be comprehensively and accurately based on the purchase, received, distributed, and disposed of substances each case independently.

State Oklahoma State Board of Pharmacy

https://nabp.pharmacy/boards-of-pharmacy/oklahoma/This is an agency of the state of Oklahoma.

Generally, this agency is tasked with regulating and controlling all pharmacy activities.

They are also responsible for licensing all pharmacists in the Oklahoma State.

It also regulates pharmaceutical laws and regulations regarding the industrial processing of drugs, selling, supply, and storage of drugs, medications, chemical compounds, and poisons.

Providing leadership and direction in the prevention and control of health-threatening drugs and foodstuffs, promoting preventable conditions, and response to public health emergencies emanating from food and drug reactions.

The Oklahoma State Board of Pharmacy ensures only professional pharmaceutical physicians are licensed to practice in the state equipment (Lawbook, 2015). Since the agency board is mandated by law enforcement, it impacts the pharmacists directly through its management of pain and Substance disorders act equipment (Lawbook, 2015).

Through this act, the Oklahoma State Board of Pharmacy ensures that pharmacists in their electronic prescription of medicine and controlled substance prescriptions are done in a manner in which there is no room for any pharmacists' errors in dispensing prescriptions equipment (Lawbook, 2015).

The Oklahoma State Board of Pharmacy also directly impacts the pharmacist's mode of drug costing hence drug price transparency. The agency ensures that the pharmacist list prices for prescription drugs, allow negotiations based on the listed rates, and ensure proper management of medical care service equipment (Lawbook, 2015). This would help in increasing transparency and accuracy in determining the price of prescriptions across the entire state.

References

Fain, K., Daubresse, M., & Alexander, G. C. (2013). The food and drug administration amendments act and postmarketing commitments. JAMA, 310(2), 202-204.

Lawbook, O. P. (2015). Oklahoma Statues, Title 59, Chapter 8. Drugs and Pharmacy (unofficial) and Title 535. Oklahoma State Board of Pharmacy (unofficial).

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US FDA: Protecting Public Health & Safety - Essay Sample. (2023, Aug 01). Retrieved from https://proessays.net/essays/us-fda-protecting-public-health-safety-essay-sample

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