Federal Food and Drug Administration. Free Essay Sample

Federal Food and Drug Administration This is a federal agency of biomedical research that focuses on essential information on the nature and conduct of living systems. The application of the above facts regarding the promotion of health, boosting the lifespan of people, and reducing illnesses through food and drug administration.

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Ideally, the agency seeks to conduct, support, and promote biomedical research on maintaining the practical health position of both human beings and animals.

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.

The agency also focuses on the security and safety of the state's nutrition supply, cosmetics, additional dietary actions, and radiator products through fostering all the significant original discoveries, advanced strategies of research, and their applications as a basis of protection and improvement of health. Food, Drug, and Cosmetic Act of 1938- the law on food, medicine, and cosmetics on Pharmaceutical practice restricted the practitioners from interstate commercial activities in misbranded and adulterated food and drinks and drugs because it majorly focused on the purity and safety (Bingham & Mallette, 2016). Besides, the law brought provisions of labeling of medicines with adequate directions and prescriptions for use. Further, the law allowed premarket approval where drug manufacturers would be approved to prove the safety of the drug before the pharmacists would start selling them to patients.

1970 Controlled Substance Act-The comprehensive drug abuse prevention directly impacted the pharmacist practices in that the requirement by law demanded every pharmacist to register, keep specific records and rules regarding the administration of controlled substances. To ensure this Act is observed, the federal legislation laid down rigid penalties for all those pharmacists who violate the controlled substance act (Bingham & Mallette, 2016). Ideally, the law requires that pharmacists to ensure prescriptions dispensed for medications must be recorded and underscored by the individual practitioner except in cases of emergency prescriptions where the pharmacist is allowed to perform oral medication (Bingham & Mallette, 2016).

Record keeping- Guides that every pharmacist must ensure the maintenance and proper keeping of medical records for two years comprehensively and accurately based on the purchase, received, distribution, and disposal of substances each case independently (Bingham & Mallette, 2016).

State Oklahoma State Board of Pharmacy Protects health, safety, and well-being of Oklahoma citizens by regulating and enforcing laws on pharmaceutical practice and the management of drugs through treatment and over the counter.

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

The board certifies the maintenance of information from the license acquisition and verification for the pharmacy practice.

Supervising pharmacy technicians to ensure that they are receiving and confirming prescription orders, preparing and counting them, and interacting with customers through answering any prescription questions from them.

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

State Board of Medical Supervision and licensure-According to the provisions of the state board of pharmacy, there shall be a composition of seven pharmaceutical physicians licensed to practice medicine in the state as representatives of the general public and four members for lay representation (Medina et al., 2020). In essence, the members of the board shall be required to be graduates from a legally chartered medical school. Non-State membership to the state board was canceled down by this law, meaning that only medical practitioners from within Oklahoma can be allowed to run pharmacies in here and join the board committee.

Management of pain and Substance disorders In October 2018, the United Staes administration under Trump signed into the law of substance use disorder prevention that demanded treatment of patients (Medina et al., 2020). This law is based on several policies of the comprehensive addiction and recovery Act that covered new initiatives for promoting prevention and accessibility to treatments. In essence, the legislation required the electronic prescription of medicine and controlled substance prescriptions to limit the pharmacists' errors in dispensing prescriptions. Additionally, it was aimed at expanding therapeutical medication management.

Drug price transparency- In this part, the pharmaceutical organizations require that every pharmacy list prices for prescription drugs, allow negotiations based on the listed rates, and ensure proper management of medical care service equipment. This would help in increasing transparency and accuracy in determining the price of prescriptions.

References

Bingham, J. T., & Mallette, J. J. (2016). Federal Bureau of Prison's clinical pharmacy program improves patient A1C. Journal of the American Pharmacists Association, 56(2), 173-177 https://www.sciencedirect.com/science/article/pii/S1544319116000777

Medina, M. S., Tran, A. L., Bhakta, K., Klatt, R. A., & Miller, J. L. (2020). Tips for writing Pharmaceutical residency letters of intent. American Journal of Health-System Pharmacy, 77(8), 605-607. https://academic.oup.com/ajhp/article-abstract/77/8/605/5814267