Prescription drug marketing definition

Prescription drug marketing means in-person meetings, mailings, telephonic conversations, video conferencing, and electronic mail activities with prescribers.
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Prescription drug marketing means any activity, including, but
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Prescription drug marketing means to provide educational or marketing
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Examples of Prescription drug marketing in a sentence

  • Prescription drug marketing is a large part of the success of the pharmaceutical industry, which grossed over $800 billion in 2011.223 Eighty percent of marketing efforts to influence physicians are through industry gifts and detailing, the activity of pharmaceutical sales representatives (reps) when they make calls to physicians and provide them with “details”—scientific 217.

  • Eligibility: All full-time faculty who work at affiliated teaching sites that constitute the SCAHEC system and who are not employees of MUSC may be considered for faculty appointments on the AHEC track.

  • Prescription drug marketing is slightly different, however, in that the person who pays for the prod- uct-the consumer-is not usually the person selecting the product.

  • These costs put consumers at risk for medical debt and bankruptcy, as each day patients are forced to choose between taking their medi- cation and paying for food, housing and other necessities.Background Prescription drug marketing, like all marketing, is intended to in- crease product sales for the com- pany.

  • A tongue-in-cheek visual representation of how “talking the whole night through” can lead to a “good morning.” Prescription drug marketing is unique in North American advertising.

  • Prescription drug marketing act.A. The requirements for wholesale distribution of prescription drugs set forth in the federal Prescription Drug Marketing Act of 1987 (21 USC §321; 21 CFR 205) are adopted by reference.B. Each wholesale distributor of prescription drugs shall comply with minimum requirements for qualifications, personnel, storage, handling, and records as set forth in the federal regulations referred to in subsection A of this section.

  • Prescription drug marketing is aimed directly to the health care provider.

  • Prescription drug marketing guidelines should be modified to improve transparency around pricing and effectivenessThe U.S. is one of just two countries in the world — the other is New Zealand15 — that allows prescription drug advertising aimed directly at the general public.


More Definitions of Prescription drug marketing

Prescription drug marketing. MEANS ANY ACTIVITY THAT DOES NOT INCLUDE CONVERSATIONS AT SCIENTIFIC CONFERENCES AND THAT MAY INCLUDE IN-PERSON MEETINGS, PHYSICAL MAILINGS, TELEPHONIC CONVERSATIONS, VIDEO CONFERENCING, ELECTRONIC MAILING OR TEXTING, OR FACSIMILE TRANSMISSIONS THAT PROVIDES EDUCATIONAL OR MARKETING INFORMATION OR MATERIALS REGARDING A PRESCRIPTION DRUG.
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Prescription drug marketing means providing to a health care entity, on behalf of 904 a pharmaceutical manufacturer, educational or marketing information or materials regarding a 905 drug that is available to a resident of the state, including through:
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Prescription drug marketing means any activity, including, but not limited to, in-person meetings, physical mailings, telephonic conversations, video conferencing, electronic mail, or facsimile, that provides educational or marketing information or materials regarding a prescription drug.
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Prescription drug marketing means to provide to a health care entity, on behalf 870 of a pharmaceutical manufacturer, educational or marketing information or materials regarding 871 a drug that is available to a resident of the state, including through:
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Related to Prescription drug marketing

  • Prescription drug means any drug required by federal law or regulation to be dispensed only

  • Prescription drug order means a lawful order of a practitioner for a drug or device for a specific patient that is communicated to a pharmacist.

  • Prescription drugs means drugs, medicine and controlled substances which by law can only be prescribed for human use by persons authorized by law.

  • Nonprescription drug or "over-the-counter drug" means any

  • Nonprescription drugs means nonnarcotic medicines or drugs which may be sold without a prescription and are prepackaged and labeled for use by the consumer in accordance with the requirements of the statutes and regulations of this state and the federal government;

  • Drug abuse means any pattern of pathological use of drugs that causes impairment in social or occupational functioning, or that produces physiological dependency evidenced by physical tolerance or by physical symptoms when it is withdrawn.

  • Participating Prescription Drug Provider means an independent retail Pharmacy, chain of retail Pharmacies, mail-order Pharmacy or specialty drug Pharmacy which has entered into an agreement to provide pharmaceutical services to participants in the benefit program. A retail Participating Pharmacy may or may not be a select Participating Pharmacy as that term is used in the Vaccinations Obtained Through Participating Pharmacies section.

  • FDA means the United States Food and Drug Administration.

  • Drug means (i) articles or substances recognized in the official United States Pharmacopoeia

  • Participating Clinical Laboratory means a Clinical Laboratory which has a written agreement with the Claim Administrator or another Blue Cross and/or Blue Shield Plan to provide services to you at the time services are rendered.

  • New Drug Application means a New Drug Application filed with the FDA in accordance with Applicable Law.

  • Rural health clinic means a rural health clinic as defined under section 1861 of part C of title XVIII of the social security act, chapter 531, 49 Stat. 620, 42 U.S.C. 1395x, and certified to participate in medicaid and medicare.

  • Marketing Authorization Application or “MAA” means an application to the appropriate Regulatory Authority for approval to sell the Product (but excluding Pricing Approval) in any particular country or regulatory jurisdiction.

  • Wholesale drug distributor means anyone engaged in the

  • Clinical laboratory means a facility for the microbiological, serological, chemical, hematological, radiobioassay, cytological, immunohematological, pathological, or other examination of materials derived from the human body for the purpose of providing information for the diagnosis, prevention, or treatment of a disease or assessment of a medical condition.

  • PDMA means the Prescription Drug Marketing Act of 1987, as amended from time to time, together with any rules or regulations promulgated thereunder.

  • Drug Master File or “DMF” is described in 21 C.F.R. Part 314.420. A DMF is a submission to the FDA that may be used to provide confidential detailed information about facilities, processes, or articles used in the manufacturing, processing, packaging, and storing of one or more human drugs.

  • FFDCA means the United States Federal Food, Drug, and Cosmetic Act, 21 U.S.C. § 301 et seq., as amended from time to time, together with any rules, regulations and requirements promulgated thereunder (including all additions, supplements, extensions, and modifications thereto).

  • MHLW means the Ministry of Health, Labour and Welfare of Japan, or the successor thereto.

  • Licensed clinical social worker means an individual who meets the licensed clinical social worker requirements established in KRS 335.100.

  • Drug addiction means a disease characterized by a

  • MFDA means the Mutual Fund Dealers Association of Canada;

  • Biological safety cabinet means a containment unit suitable for the preparation of low to moderate risk agents where there is a need for protection of the product, personnel, and environment, according to National Sanitation Foundation (NSF) Standard 49.

  • Prescription monitoring program means the electronic system within the Department of Health Professions that monitors the dispensing of certain controlled substances.

  • Federal Health Care Program has the meaning set forth in 42 U.S.C. 1320a-7b(f).

  • ERCOT Protocols means the document adopted by ERCOT, including any attachments or exhibits referenced in that document, as amended from time to time, that contains the scheduling, operating, planning, reliability, and Settlement (including Customer registration) policies, rules, guidelines, procedures, standards, and criteria of ERCOT. For the purposes of determining responsibilities and rights at a given time, the ERCOT Protocols, as amended in accordance with the change procedure(s) described in the ERCOT Protocols, in effect at the time of the performance or non-performance of an action, shall govern with respect to that action.