コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 game theory (auctions), and social networks (marketing).
2 nce through technological processes prior to marketing.
3 used to inform protected area management and marketing.
4 ay offer a partial view of exposed off-label marketing.
5 on physicians and traditional pharmaceutical marketing.
6 education, financial modeling, policing, and marketing.
7 pathways do not exist to guide research and marketing.
8 ssue for research, nutritional labelling and marketing.
9 rove living standards, and enhance livestock marketing.
10 as where ranking has a role, from science to marketing.
11 mbine several policy tools and strong social marketing.
12 d Drug Administration over its first year of marketing.
13 exponential growth driven mainly by creative marketing.
14 ulation of consumer and professional medical marketing.
15 tritional quality of EVOOs and improve their marketing.
16 s of policies that address affordability and marketing.
18 employees relative to the Prescription Drug Marketing Act or the False Claims Act and probationary s
19 ty to one violation of the Prescription Drug Marketing Act, settled claims related to alleged violati
20 his study are relevant for understanding how marketing actions can affect consumer choice behavior as
21 e paper provides evidence for the ability of marketing actions to modulate neural correlates of exper
23 leblower complaints as involved in off-label marketing activities adequately disclosed their conflict
24 em was an important driving factor for these marketing activities, Medicare has shifted to an Average
26 using community-based distributers as social marketing agents and incorporating financing systems to
28 Despite the importance and pervasiveness of marketing, almost nothing is known about the neural mech
29 und 46 was halted due to the contemporaneous marketing and clinical withdrawal of other centrally act
30 evelopment, and creating efficiencies in the marketing and distribution of educational materials and
31 , we evaluated the effect of community-based marketing and distribution of Sprinkles MNP on childhood
32 ve proven immensely useful in fields such as marketing and earth sciences, public health is still rel
34 on that upgraded the supply chain (combining marketing and home delivery), provided rebates and finan
35 osition, botanical aspects, pharmacological, marketing and nutrition of these species based on studie
38 r advertisements; prohibiting youth-oriented marketing and sales; prohibiting child-friendly ENDS fla
39 ene therapy medicines have been licensed for marketing and several more are advancing toward that goa
41 mplicit positive associations with junk food marketing and substantially improves boys' daily dietary
42 ributed in part to the perception created by marketing and the popular press that they are safer than
43 clinical and regulatory decisions about the marketing and use of new treatments, these assumptions m
45 kage warning labels, restrict child-directed marketing, and ban sales in schools of all foods and bev
49 cco products; regulation of the advertising, marketing, and promotion of tobacco products; regulation
52 d by the US Food and Drug Administration for marketing, and several others are in various stages of d
53 the dense built environment, pervasive food marketing, and the increased availability of energy-dens
57 n of failed applications is costly, delaying marketing approval and the availability of new drugs to
59 ugs received US Food and Drug Administration marketing approval for acute myeloid leukemia (AML) trea
60 t thrombin inhibitor dabigatran has received marketing approval from the European Medicines Agency.
62 rocesses that supported drug development and marketing approval of DAAs for treatment of hepatitis C,
64 ccess rates, with over 40% of INDs obtaining marketing approval, in a median time of about six years
65 f an anticancer agent at the time of initial marketing approval, sponsors customarily collect compreh
66 without industry champions to bring them to marketing approval, there may be justification for a mor
68 on and sale of these data for pharmaceutical marketing are currently the subjects of legislation in s
69 n intervention that frames manipulative food marketing as incompatible with important adolescent valu
70 cipants rated scenarios in which the use was marketing as less appropriate than when the use was rese
71 o establish a monopoly, it planned intensive marketing, as if in a competitive market, aiming to targ
72 afer or more effective new drugs and greater marketing associated with higher intraclass list prices.
73 ted approval pathways, including conditional marketing authorisation (CMA) and accelerated assessment
74 s of clinical investigation or have received marketing authorisation for adults; however, none have d
76 A), speed up European Medicines Agency (EMA) marketing authorisation recommendations for medicinal pr
81 umors, with (177)Lu-DOTATATE having acquired marketing authorization in Europe and the United States.
83 needed before considering a revision of the marketing authorization process for antibacterial generi
84 driving basic immunological research and for marketing authorization purposes by regulatory authoriti
85 nt phenolic antioxidant from rosemary with a marketing authorization, spontaneously forms a relativel
86 ffectiveness of interventions addressing the marketing, availability, and price of healthy and unheal
89 y illustrates the relative importance of the marketing based benefits that accrue to Leadership in En
94 oS displays will prevent this means of price marketing but our study also suggests that minimum prici
95 ed during the first two years of natalizumab marketing but, by the end of November, 2009, 28 cases ha
97 Research and scholarship were also used for marketing by encouraging "key customers" to participate
98 eight loss centers or for direct-to-consumer marketing by manufacturers and does not apply to patient
100 pragmatic use and validation, we carry out a marketing campaign that shows a threefold increase in re
102 t from the support of educational and social marketing campaigns developed with governmental input an
103 wer testimony have alleged complex off-label marketing campaigns that remain concealed to company out
104 bacco products, smoke-free policies, counter-marketing campaigns, advertising restrictions, augmentin
107 ry hurdles, which might prevent vendors from marketing cardiac MR perfusion imaging, may have hampere
108 ntify, document, and analyze U.S. businesses marketing "cell therapy" for ocular conditions as of Sep
109 ns of median price per ounce on the basis of marketing claims (eg, dermatologist recommended, fragran
110 However, an examination of Internet-based marketing claims revealed widespread promotion of such i
112 ovement in the transparency of local seafood marketing compared to previous studies, the results rema
113 s that pass along research, development, and marketing costs to the consumer; providers of cancer car
114 ns of neuroscience to such diverse arenas as marketing, criminal justice, the military, and worker pr
115 acilitate the production of comparative post-marketing data by investing in the development of collab
116 division handled both the scientific and the marketing data, including collection, analysis, and diss
117 (InfoGroup, Papillion, Nebraska) commercial marketing database for neighborhood control recruitment
120 them in domains as diverse as epidemiology, marketing, development economics, and public health.
121 on to fulfill a marketing objective; Merck's marketing division handled both the scientific and the m
122 ey themes: The trial was designed by Merck's marketing division to fulfill a marketing objective; Mer
123 AGE was a seeding trial developed by Merck's marketing division to promote prescription of Vioxx (rof
124 he recent surge in direct-to-consumer device marketing, do-it-yourself enthusiasm, and an escalating
128 asible waste stream option and a sustainable marketing edge while treading the path toward a circular
129 For decades methodologists in psychology, marketing, education, and survey research have studied t
130 apers, documents were found describing Merck marketing employees developing plans for manuscripts, co
136 blower complaints alleging illegal off-label marketing from the US Department of Justice and other pu
137 d patients has been widespread, but how this marketing has contributed to the diffusion of the techno
139 ed, participate in direct-to-consumer online marketing, have websites that can be data-mined with con
140 pain management, ethical lapses in corporate marketing, historical stigmas directed against people wh
141 d exposure to environmental cues (e.g., food marketing); however, the mechanisms that link these fact
143 ry and only two contained elements of social marketing in the design, although five addressed sustain
145 ber of new antibiotics annually approved for marketing in the United States continues to decline.
146 ber of new antibiotics annually approved for marketing in the United States has reversed its previous
147 three rHuEPO products that are approved for marketing in the US or EU as biosimilars, and eight rHuE
152 cal acceptability of interactions; perceived marketing influence; perceived reliability of industry i
153 its collected and the use of recruitment and marketing initiatives that appeal to the increasingly di
155 ntervention stores received a 6-mo, in-store marketing intervention that promoted the sales of health
156 or spending and number of ads); professional marketing (IQVIA Institute for Human Data Science, Open
161 ood policies are warranted to support social marketing messages and to reduce the cultural and econom
162 or reaching physicians, allowing delivery of marketing messages at the point of care, when clinical d
163 consumption trends consistent with industry marketing models would be expected to increase the impac
164 ), school-based programs (n = 2), and social marketing (n = 2) (2 interventions tested multiple appro
165 alysis, and dissemination; and Merck hid the marketing nature of the trial from participants, physici
166 d by Merck's marketing division to fulfill a marketing objective; Merck's marketing division handled
167 a scientific question but primarily fulfill marketing objectives, have not been described in detail.
169 wn of the twentieth century, coincident with marketing of aspirin-a signature event in the history of
171 rt has been expended to restrict the adverse marketing of breastmilk substitutes, similar effort now
173 tensivists to remain in the field, proactive marketing of critical care, and expanded engagement by t
174 From 1997 through 2016, spending on medical marketing of drugs, disease awareness campaigns, health
175 pipe tobacco smoking has been abetted by the marketing of flavored tobacco, a social media environmen
177 One alternative explanation is that the marketing of high-sugar foods, especially sugar-sweetene
178 fruit which often results in harvesting and marketing of inedible, immature or over ripe berries.
180 ciated with the development, production, and marketing of new drugs and technologies, many of which a
183 are changing with increased availability and marketing of packaged and fast foods and sugar-sweetened
184 d inform the development, manufacturing, and marketing of pediatric medications for resource-limited
185 der children from increasingly sophisticated marketing of sedentary activities and energy-dense, nutr
186 ns, these findings suggest that labeling and marketing of some products which claim to provide these
187 eir availability in schools; restrictions on marketing of sugary foods to children; public awareness
190 atform, along with a manual search, from the marketing of the first PGA, latanoprost, in 1995 to the
194 g tobacco industry influence on taxation and marketing of tobacco; we included 45 of 46 papers in the
196 oduce legislation to restrict the commercial marketing of unhealthy foods and beverages to children.W
199 asure the effects of nontraditional forms of marketing on the health-related behaviors of children.
200 do not require clinical studies before their marketing or formal approval from regulatory agencies, a
201 that most medicines that were withdrawn from marketing or received a black-box warning because of hep
205 e evaluation of clinical benefit in the post-marketing period should be limited to instances when the
206 manufacturers to conduct studies in the post-marketing period, these studies might remain incomplete
213 nd state investigations of allegedly illegal marketing practices of other pharmaceutical firms and ha
214 iversity and/or government groups employ the marketing practices of pharmaceutical companies to impro
215 ct placement/choice architecture, innovative marketing practices, menu and product labeling, worksite
216 ng countries by teaching basic financial and marketing practices, yet the impacts of such programs ar
219 ollect double red blood cell units; targeted marketing programs to provide effective messages; season
220 tine, and many ECIG manufacturers have begun marketing protonated nicotine products, often with high
221 are taking advantage of widespread fears by marketing purported stem cell treatments for COVID-19.
222 n based on the sales network, the price, the marketing quality and the presence of filters in the pac
223 ate on the implementation of sugar taxation, marketing regulation, and other sugar-related policies.
224 ure on tobacco industry efforts to influence marketing regulations and develops taxonomies of 1) indu
225 nce to tobacco industry efforts to influence marketing regulations; supported claims with verifiable
226 an injectable clinical biomaterial must meet marketing, regulatory, and financial constraints to prov
227 ng ultrasound contrast agents following post-marketing reports of 4 patient deaths that were temporal
228 (gift policies, r = 0.28, 95% CI 0.11-0.44; marketing representative access policies, r = 0.51, 95%
229 0.19-1.04) and less likely to interact with marketing representatives (AMSA score, OR 0.33, 95% CI 0
230 students' gift acceptance, interactions with marketing representatives, and perceived adequacy of fac
232 lacement therapy (PERT) to have approval for marketing, rescinding the distribution of PERT that had
235 ethods from operation risk index analysis in marketing research to develop a formula that considers a
236 overnment have instituted self-regulation of marketing, research in the psychology and social science
237 ere thus subject to the law's warning label, marketing restriction, and school sales ban policies.
238 een nutrient profile (NP) models relevant to marketing restrictions by applying them in the Canadian
239 mandated front-of-package warning labels and marketing restrictions for unhealthy foods and beverages
240 ncreases, 14% by smoke-free air laws, 14% by marketing restrictions, 8% by health warnings, 6% by mas
241 , smoke-free air laws, mass media campaigns, marketing restrictions, packaging requirements, cessatio
243 ss authorized the FDA to grant extensions of marketing rights known as "pediatric exclusivity" if FDA
244 tration (FDA) to grant 6-month extensions of marketing rights through the Pediatric Exclusivity Progr
247 tion are needed to prevent the inappropriate marketing, sale, and clinical use of unlicensed botulinu
248 e apparent strategic goals of each off-label marketing scheme and the practices consistent with those
249 e findings are consistent with the idea that marketing self-regulation has failed to keep television
250 on-level cohort study using Intercontinental Marketing Services Health Canada's data from June 2003 t
252 ng their financial interests) such as social marketing, social franchising, vouchers, and contracting
253 ethylene pathway, and innovative storage and marketing solutions for current and novel fruit cultivar
256 and using more sophisticated recruitment and marketing strategies as well as automated collection tec
257 research on this topic has mainly focused on marketing strategies for garnering public acceptance of
258 t is possible for programmes to adopt modern marketing strategies that are attractive to healthy clie
260 veness of utilizing personalized direct-mail marketing strategies to promote organ donation with an e
262 tudy was to evaluate the effects of in-store marketing strategies to promote the purchase of specific
263 -the present campaign employed a direct-mail marketing strategy that registered 6908 individuals in t
268 ing With Emboli Protection Surveillance-Post-Marketing Study) multicenter, prospective, single-arm, s
269 ve measurement of adoption to inform design, marketing, subsidies, finance, or dissemination practice
270 pproach that utilizes clinical SEs from post-marketing surveillance and the drug label to predict 1,5
272 EGF agents will only be achieved though post-marketing surveillance or through the interrogation of h
274 In a non-interventional, observational, post-marketing surveillance study, patients with an establish
275 ed with trends on clinical outcomes and post-marketing surveillance to assess safety, serve as the fo
277 Changes to these device approval and post-marketing systems must be accompanied by ongoing researc
279 bacco control policies should prohibit price marketing that otherwise erodes the full impact of such
280 dronic acid received regulatory approval for marketing, the FDA received reports of nine patients wit
281 Although these initiatives need improved marketing, the Society of Critical Care Medicine members
282 st half of prepackaged foods as eligible for marketing to children [49.0% (95% CI: 48.2%, 49.8%)].
283 oportion of foods that would be eligible for marketing to children was calculated with the use of eac
286 s can be learned and principles applied from marketing to highlight the potential pitfalls of current
290 communities in rural Bangladesh to different marketing treatments-community motivation and informatio
293 Mean ratings ranged from a low of 3.81 for a marketing use when consent was not obtained and specific
294 ere rated as more appropriate than consented marketing uses (5.65 vs. 4.52; difference, 1.13 [CI, 0.8
296 The UK self-regulatory system for exposing marketing violations relies largely on complaints from c
300 th Food and Drug Administration approval for marketing - Y(90) ibritumomab tiuxetan and I(131) tositu