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Overview of the Problem In a perfect setting, health care providers would be capable of constantly projecting and ordering the correct volume of drugs in a prompt way so that drug companies could manufacture adequate volumes and distributors could distribute the products in a timely way.... At times production deficiencies arise when drug companies miscalculate the demand for products due to newly implemented treatment policies, new symptoms, changes in medical procedure, and low-quality planning....
15 Pages
(3750 words)
Research Paper
When a drug is out of the patent protection (no longer protected by patent), the company may sell the products under whichever name they want common name or business name.... drugs frequently have several terms.... hen the drug is accepted by the administration agency liable for making sure that the drugs being marketed in the country are not dangerous and efficient, it is provided with a generic (official) title and a business (proprietary or brand) title....
5 Pages
(1250 words)
Research Paper
Consumers and health care providers are the parties involved in the decision-making process.... CPS should place into consideration the concerns raised over new weight loss drugs and focus on providing solutions to solve any problems that may arise.... Secondly, after an overweight patient is aware of their condition, they are required to start an exercising program and ask health care providers for assistance when they need it.... Lastly, if all the other methods fail, the health care providers can recommend the use of the Metabical drug under observation....
5 Pages
(1250 words)
Case Study
Since herb-drug interaction is highly likely, government health, and food and drugs sectors should start regulating herbal products, and health care practitioners should be aware of such interactions so that they could advise their patients about it.... Despite this, governments are not regulating these products nor are they checking its effectiveness and toxicity.... The Food and Drug Administration classify them as dietary supplements; hence, no regulations are placed upon the products (Bressler, 2005)....
36 Pages
(9000 words)
Essay
The paper "Consumer Trends of Drug against Headaches and Pains of the Body Parts" states that Advil drug manufacturing companies should consider expanding their consumer market, through embracing strategies aimed at exporting their drug products all over the world and in developing countries.... he latter enhances an individual's perceptions of the positive relieving effects of the ibuprofen products on muscles and body pains.... From 1984 to date, Advil painkiller has faced market competition from other painkiller drugs such as Vanquish and aspirin drugs, with Tylenol being the major competitor in the pharmaceutical market....
7 Pages
(1750 words)
Essay
The respective agencies protect public health by ensuring that only products with favorable benefits to risk profiles are licensed.... Product Assessment: All medicinal products need to be licensed before they can be marketed unless they meet one of a small number of exemptions.... Most importantly, it is a process involving the constant percolation of data through rigorous filters strewn with tribulations and complicated by the difficulty of making decisions that affect human health when all the facts are not known....
6 Pages
(1500 words)
Essay
When a drug is out of the patent protection (no longer protected by patent), the company may sell the products under whichever name they want the common name or business name.... This paper "Strategic Options for Brand-Name Prescription drugs When Patents Expire" focuses on the fact that drugs frequently have several terms.... The drug is accepted by the administrative agency liable for making sure that the drugs being marketed in the country are not dangerous and efficient....
6 Pages
(1500 words)
Research Paper
n this second phase, SFDA utilizes an electronic system in the form of Saudi Drug Registration to facilitate registration of medicinal, herbal, and health products for veterinary as well as human use.... There are three critical applications in this stage: Marketing Authorization Application of Medicinal Product for Human Use, MAA of Herbal and health Product, and MAA of Medicinal Product for Veterinary Use.... Some processes or documents are required only in SFDA as Alcohol and Pork-Free declaration must be mentioned in the CTD module 1 and manufacturers that want to register their products in SFDA must meet Saudi's GMP....
7 Pages
(1750 words)
Article