Final answer:
The Food and Drug Administration (FDA) is responsible for ensuring proper temperature controls and developing written policies for proper storage of RX drugs, as well as enforcing laws regarding drug safety and effectiveness. They also review and regulate drug advertising and promotion. Despite the protection this provides, some patients and pharmaceutical companies may experience negative consequences due to the stringent regulations.
Step-by-step explanation:
The entity responsible for ensuring proper temperature controls and developing/maintaining written policies and procedures to ensure proper storage of RX drugs is the Food and Drug Administration (FDA). The FDA is crucial in regulating the safety, efficacy, and security of drugs, overseeing everything from long-term storage to short-term temperature stability and post-preparative stability. They enforce laws to maintain the purity and effectiveness of medications, and conduct inspections to oversee the production and shipment of pharmaceutical products. In addition to this, the FDA's Office of Prescription Drug Promotion actively reviews and regulates prescription drug advertising and promotion to further ensure public health is safeguarded.
While the FDA's strict regulations protect the public from unsafe drugs, the anonymous losers in this scenario can be the patients who suffer from the delay in getting potentially lifesaving drugs while they undergo extensive testing, or the pharmaceutical companies that incur the high costs and time investments associated with bringing a new drug to market. Moreover, the Federal Trade Commission (FTC) works alongside the FDA by regulating advertising and promotion for over-the-counter drugs, thus ensuring consumers receive truthful information about these products.