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Pharmaceutical Direct to Patient Marketing

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PHARMACEUTICAL DIRECT TO CONSUMER MARKETING
Grand Canyon University: 437V
September 18, 2013

Current medical and pharmaceutical marketing strategies raise concern from consumer groups and the medical community due to the overconsumption of the products as well as the advertised products supplying no medical benefit to the consumer. Although the companies’ marketing strategies of medical and pharmaceutical products attempt to persuade the public that the products are revolutionary and life changing, the marketing strategies exclude pertinent information that may change the consumer’s minds about purchasing the products being offered. Many consumers purchase products that assert testimony of anti-aging effects in an attempt to regain what was once lost from the natural human aging process. Other consumers search for answers and treatment to a wide variety of medical conditions or ailments and these revolutionary products are then viewed as the essential answer to the consumer’s search. An ethical dilemma currently exists with the current medical and pharmaceutical marketing strategies and approaches with desperate need for the consumer to be knowledgeable about all aspects of the products being marketed and the government or influential bodies to be reactive to the current marketing strategies.
Regulatory Bodies of Marketing for Pharmaceutical Companies The Division of Drug Marketing, Advertising, and Communications (DDMAC), a sub division of the Food and Drug Administration (FDA) have regulated all prescription drug ads since 1962 (FDA, 2013). In 2011 the FDA gave its Office of Medical Policy an upgrade, making it a “super office” and giving the department formerly known as the DDMAC, a new acronym: OPDP for The Office of Prescription Drug Promotion. Most ads that DDMAC first regulated contained mostly journal ads that were targeted at health care

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