ライフサイエンスコーパス: ethics committee

1 al studies were approved by the local animal ethics committee.

2 The study was approved by the local ethics committee.

3 ospective study was approved by the regional ethics committee.

4 tive study was approved by the institutional ethics committee.

5 inistry of Health and by the local competent ethics committee.

6 protocol was approved by the regional animal ethics committee.

7 All procedures were approved by the animal ethics committee.

8 This study was approved by an independent ethics committee.

9 The protocol was approved by the ethics committee.

10 ilot study was approved by the institutional ethics committee.

11 ethical approval of the Nottingham Research Ethics Committee.

12 dy was approved by the institutional medical ethics committee.

13 rol study was approved by the local research ethics committee.

14 re approved by the Utrecht University Animal Ethics Committee.

15 d the study was approved by an institutional ethics committee.

16 vely acquired data was approved by the local ethics committee.

17 e study protocol was approved by the medical ethics committee.

18 y protocol was approved by the institutional ethics committee.

19 d, and the Australian Defense Human Research Ethics Committee.

20 filled the requirements of the institutional ethics committee.

21 on of Helsinki and was approved by the local ethics committee.

22 The study was approved by our ethics committee.

23 prospective study was approved by the local ethics committee.

24 study protocol was approved by institutional ethics committee.

25 the institutional review board and the local ethics committee.

26 Methods The study was approved by the local ethics committee.

27 protocol was approved by the local research ethics committee.

28 compliant study was approved by the regional ethics committee.

29 Methods Approval was obtained from the local ethics committee.

30 should be overseen by a functional research ethics committee.

31 This study was approved by the local ethics committee.

32 nimal experiments were approved by the local ethics committee.

33 from the psychiatry service and the hospital ethics committee.

34 analysis was approved by the local research ethics committee.

35 longitudinal trial and approved by the local ethics committee.

36 Each treatment was approved by the clinical ethics committee.

37 tive study was approved by the institutional ethics committee.

38 by the institutional review board and local ethics committee.

39 The study protocol was approved by the local ethics committee.

40 trospectively analyzed after approval by the ethics committee.

41 his study was approved by the local research ethics committee.

42 the study was approved by the local research ethics committee.

43 on of Helsinki and was approved by the local ethics committee.

44 arch projects have been examined by research ethics committees.

45 the University of Zambia Biomedical Research Ethics Committee (011-04-12).

46 With the approval of the local ethics committee, 100 consecutive patients (mean age, 61

47 Following approval by the ethics committee, a long-term supplementation treatment

48 After study approval by the local ethics committee, all participants provided written info

49 l approval was granted by the local research ethics committee; all participants gave written consent.

50 This study was approved by the regional ethics committee; all patients gave written informed con

51 The case-control study was approved by local ethics committees; all patients signed informed consent.

52 Consultation from ethics committees also may be helpful in achieving resol

53 The study was approved by the medical ethics committee and all subjects gave written informed

54 etrospective study was approved by the local ethics committee and compliant with the Declaration of H

55 and Methods This prospective study had local ethics committee and German Federal Institute for Drugs

56 This study was approved by the local ethics committee and informed consent was obtained from

57 The study was approved by local ethics committee and informed consent was obtained from

58 The study was approved by the research ethics committee and informed consent was obtained.

59 evaluation of data was approved by the local ethics committee and informed consent was waived.

60 study was approved by the Cantonal Research Ethics Committee and informed written consent was obtain

61 s and the Cancer Imaging Archive after local ethics committee and institutional review board approval

62 aised by the independent data monitoring and ethics committee and only five patients were withdrawn f

63 study was approved by the local research and ethics committee and patient informed consent was obtain

64 tes evolved through the joint efforts of the Ethics Committee and the Board of Directors.

65 was approved by the Academic Medical Center Ethics Committee and the Great Ormond Street Hospital Et

66 Methods The study was approved by the local ethics committee and the local Veterinary Office.

67 case-control study was approved by the local ethics committee and the research department of Nottingh

68 With the approval of the Hospital Ethics Committee and waiver of the informed consent requ

69 The study was approved by the institutional ethics committee and was conducted according to principl

70 study was approved by the national research ethics committee and was performed with informed consent

71 With the permission of the local ethics committee and with informed written consent, 106

72 the Newcastle and North Tyneside 2 Research Ethics Committee and with written consent.

73 proval of the Newcastle and North Tyneside 2 ethics committee and written consent.

74 er obtaining approval from the institutional ethics committee and written informed consent from the p

75 etrospective study was approved by the local ethics committee and written informed consent was obtain

76 TERIALS AND Approval from the local research ethics committee and written informed consent were obtai

77 rious adverse events (SAEs) were reported to ethics committees and a central safety monitor.

78 Clinical ethics committees and clinical ethicists can act as a us

79 f the full Society of Critical Care Medicine Ethics Committees and the Society of Critical Care Medic

80 prospective study was approved by the local ethics committee, and all 20 adult patients provided inf

81 The study was approved by the local research ethics committee, and all participants gave written info

82 This study was approved by the ethics committee, and all participants gave written info

83 The study was approved by a regional ethics committee, and all participants provided written

84 valuation Trial II study was approved by the ethics committee, and all participants provided written

85 this study was approved by the institutional ethics committee, and all patients gave informed consent

86 This study was approved by the regional ethics committee, and all patients gave informed consent

87 The study was approved by the regional ethics committee, and all patients gave written consent.

88 The study was approved by the regional ethics committee, and all patients gave written informed

89 Methods The study was approved by the local Ethics Committee, and all patients or their parents gave

90 AA-compliant study was approved by the local ethics committee, and all patients provided informed con

91 This study was approved by the local ethics committee, and all patients provided written info

92 The study was approved by the local ethics committee, and all patients provided written info

93 tudy was approved by the Royal Free Research Ethics Committee, and all subjects gave full written inf

94 Methods The study was approved by the local ethics committee, and all subjects gave written informed

95 The study was approved by the local ethics committee, and all subjects gave written informed

96 This study was approved by the local ethics committee, and informed consent was obtained from

97 The study was approved by the local ethics committee, and informed consent was obtained from

98 en by the University College London Hospital ethics committee, and informed consent was obtained from

99 tudy was approved by the local institutional ethics committee, and informed consent was obtained from

100 tive study was approved by the institutional ethics committee, and informed consent was waived.

101 study was approved by the hospital research ethics committee, and informed written consent was obtai

102 Methods The study was approved by a research ethics committee, and participants gave written informed

103 The study was approved by the local ethics committee, and patients gave written informed con

104 ional study was approved by an institutional ethics committee, and the need for patient consent was w

105 quired data was approved by an institutional ethics committee, and the requirement for informed conse

106 ve data evaluation was approved by the local ethics committee, and the requirement to obtain informed

107 hods This two-part study was approved by the ethics committee, and written consent was obtained from

108 tive study was approved by the institutional ethics committee, and written informed consent was acqui

109 This study was approved by the local ethics committee, and written informed consent was obtai

110 prospective study was approved by the local ethics committee, and written informed consent was obtai

111 This study was approved by the local ethics committee, and written informed consent was obtai

112 ective study was approved by the appropriate ethics committee, and written informed consent was obtai

113 This prospective study was approved by the ethics committee, and written informed consent was obtai

114 The study was reviewed and approved by the ethics committee, and written informed consent was obtai

115 This in vivo study was approved by the local ethics committee, and written informed consent was obtai

116 s This prospective study was approved by our ethics committee, and written informed consent was obtai

117 The study was approved by the local ethics committee, and written informed consent was obtai

118 AA-compliant study was approved by the local ethics committee, and written informed consent was obtai

119 case-control study was approved by the local ethics committee, and written informed consent was waive

120 study was approved by the national research ethics committee, and written patient consent was obtain

121 cluding researchers, regulatory authorities, ethics committees, and policymakers.

122 prospective study was approved by the local ethics committees, and written informed consent was obta

123 Local research ethics committee approval and informed consent were obta

124 Research ethics committee approval and informed consent were obta

125 Ethics committee approval and informed consent were obta

126 Materials and Methods Institutional ethics committee approval and informed consent were obta

127 Ethics committee approval and informed consent were obta

128 With ethics committee approval and informed consent, mammogra

129 MATERIALS AND Institutional ethics committee approval and parental informed consent

130 MATERIALS AND Ethics committee approval and patient informed consent w

131 Research ethics committee approval and patient written informed c

132 erformed between 2006 and 2016 with research ethics committee approval and written informed consent f

133 Local ethics committee approval and written informed consent w

134 Institutional ethics committee approval and written informed consent w

135 Research ethics committee approval and written informed consent w

136 Methods Institutional review board and local ethics committee approval and written informed consent w

137 re enrolled prospectively in the study after ethics committee approval and written informed consent.

138 The study was performed with local research ethics committee approval and written informed parental

139 Materials and Methods The study received ethics committee approval for animal experimentation.

140 otocol had the appropriate national research ethics committee approval for the countries where the st

141 ter 1997 (P =.05), and JAMA did not describe ethics committee approval in 25 (42%) before 1997 vs 13

142 nical trials obtained the appropriate IRB or Ethics Committee approval prior to enrolling any patient

143 Institutional ethics committee approval was given, and informed consen

144 Research ethics committee approval was granted to record eye-trac

145 Local ethics committee approval was granted, and written infor

146 No ethics committee approval was needed.

147 53 (18%) published after 1997 (P =.01), and ethics committee approval was not mentioned in 93 (31%)

148 Materials and Methods Local ethics committee approval was obtained at all sites for

149 Formal ethics committee approval was obtained for the study, an

150 Research ethics committee approval was obtained for this study, a

151 Local research ethics committee approval was obtained with written cons

152 Local ethics committee approval was obtained, and 34 patients

153 Internal ethics committee approval was obtained, and patients gav

154 Institutional review board/ethics committee approval was obtained.

155 Local research ethics committee approval was obtained; informed consent

156 Institutional ethics committee approval was received for this prospect

157 s Written informed consent and institutional ethics committee approval were obtained.

158 d consent and multicenter and local research ethics committee approval were obtained.

159 The study received ethics committee approval, and all women gave written in

160 With ethics committee approval, data from the Trauma Registry

161 With ethics committee approval, records for 103 consecutive p

162 129)Xe were performed with National Research Ethics Committee approval, with informed consent from th

163 The study protocol had institutional ethics committee approval, with written informed consent

164 tudy was HIPAA-compliant with local research ethics committee approval.

165 udy had institutional review board and local ethics committee approval.

166 rate of reporting on informed consent and on ethics committee approval.

167 als and Methods This study had institutional ethics committee approval.

168 elsinki and was performed according to local ethics committee approval.

169 oved their reporting on informed consent and ethics committee approval; however, 9% of studies still

170 MATERIALS AND This study design had hospital ethics committee approval; informed consent was waived.

171 This study was granted institutional ethics committee approval; the need for patient consent

172 ccessed the detail presented on the Research Ethics Committee approved participant information sheet

173 In addition, the ethics committee approved the retrospective evaluation o

174 spectively registered on January 12th, 2018; Ethics Committee approved the study (ID: 1.790.088) on O

175 A local ethics committee approved the study and all patients gav

176 The institutional ethics committee approved the study and waived informed

177 Materials and Methods The institutional ethics committee approved the study and waived the requi

178 The Lithuanian Regional Ethics Committee approved the study protocol (permission

179 The institutional ethics committee approved the study protocol, and all pa

180 A local ethics committee approved the study, and all subjects ga

181 The institutional research ethics committee approved the study, and parental consen

182 The institutional ethics committee approved the study, and written informe

183 The local research ethics committee approved the study, and written informe

184 Local ethics committee approved the study, with patient inform

185 The institutional ethics committee approved the study.

186 ided written informed consent, and the local ethics committee approved the study.

187 vided signed consent, and the local research ethics committee approved the study.

188 The institutional ethics committee approved the use of this protocol.

189 The local ethics committee approved this prospective study, and wr

190 Materials and Methods The ethics committee approved this retrospective multicenter

191 The ethics committee approved this retrospective single-cent

192 The institutional ethics committee approved this retrospective study and g

193 The institutional ethics committee approved this retrospective study, with

194 The institutional ethics committee approved this study and waived informed

195 The local ethics committee approved this study, and all subjects g

196 An institutional ethics committee approved this study, and informed conse

197 The local ethics committee approved this study, and informed paren

198 The local ethics committee approved this study, and oral informed

199 The local research ethics committee approved this study, and the subjects a

200 The local research ethics committee approved this study, and written consen

201 The local ethics committee approved this study.

202 The responsible justice department and ethics committee approved this study.

203 his study was institutional review board and ethics committee approved.

204 Institutional and regional medical ethics committees approved the study, and all patients s

205 Local ethics committees approved the study; all participants g

206 As part of the ethics-committee approved Dutch-Belgian Randomised Lung

207 This was an ethics committee-approved multicenter study.

208 d consent to participate in this prospective ethics committee-approved study.

209 itten informed consent was obtained for this ethics committee-approved study.

210 from all participants in this institutional ethics committee-approved study.

211 re retrospectively included in this regional ethics committee-approved study.

212 tten informed consent for this institutional ethics committee-approved study.

213 smaller were included in this institutional ethics committee-approved study.

214 registered at the Witten/Herdecke University Ethics Committee as 140/2016 and retrospectively registe

215 owel disease, and were judged by the medical ethics committee as not being related to the therapy.

216 This prospective study was approved by the ethics committee at a university hospital and was conduc

217 Methods This study was approved by the local ethics committee at all participating sites.

218 ved by the institutional review board and/or ethics committee at each site.

219 pproved by the institutional review board or ethics committee at each study site and was compliant wi

220 ealthcare institutional review board and the Ethics Committee at Hopital Albert Schweitzer approved t

221 This study was approved by the ethics committee at the institution.

222 s granted by the Faculty of Science Research Ethics Committee at the University of Bristol.

223 The Ethics Committees at both hospitals and the Institutiona

224 s, including representation on institutional ethics committees, attitude research with individuals fr

225 archived protocols approved by six research ethics committees between 13 January 2000 and 25 Novembe

226 mmittee and the Great Ormond Street Hospital Ethics Committee; both committees waived the requirement

227 As Ethics Committee Chair, I am pleased to introduce the fi

228 sed clinical trial, most data-monitoring and ethics committees (DMECs) rely on the p value for the di

229 tors, statisticians, and data monitoring and ethics committees face when the factors that affect the

230 The study was approved by the regional ethics committee for animal care.

231 nimal experiments were approved by the local ethics committee for animal experiments.

232 hods The protocol was approved by the French Ethics Committee for Animal Experiments.

233 2019 after receiving authorization from the ethics committee for health research.

234 The study was approved by the ethics committee for studies in humans and the animal ca

235 Approval was waived by the local ethics committee for this retrospective study.

236 exemption was granted by the local research ethics committee for this retrospective study.

237 This is not a conventional ethics committee, frequently giving rise to a board's bu

238 The National Health Service West Glasgow Ethics Committee granted approval for this study.

239 ten consent according to institutional human ethics committee guidelines.

240 l Health Service Central Office for Research Ethics Committee guidelines; informed patient consent wa

241 as approved by the University of Otago Human Ethics Committee (Health; Reference Number HD14/42).

242 The Ethics Committee hopes this column will be the first of

243 nt guidelines and regulations of the medical ethics committee in Hospital of Stomatology, Hebei Medic

244 rotocols approved between 2000 and 2003 by 6 ethics committees in Canada, Germany, and Switzerland we

245 idelines for further development of research ethics committees in El Salvador.

246 tive study was approved by the institutional ethics committee; informed consent was obtained from all

247 This study was approved by the local ethics committees; informed consent was obtained.

248 efore it would be appropriate for a research ethics committee/institutional review board to approve o

249 l (Boston, MA, USA) and the Rwandan National Ethics Committee (Kigali, Rwanda).

250 receiving approval from the clinical studies Ethics Committee, magnetic resonance imaging (MRI) studi

251 roved by the UK Ministry of Defence research ethics committee (MODREC 165/Gen/10 and 692/MoDREC/15).

252 The local ethics committee of animal experimentation approved all

253 Animal Ethics Committee of Botucatu Medical School - Certificat

254 istry The study protocol was approved by the Ethics Committee of Qom University of Medical Sciences (

255 y protocol was approved by the institutional ethics committee of the coordinating center on behalf of

256 is HIPAA-compliant study was approved by the ethics committee of the institution, and all patients pr

257 ith HIPAA guidelines and was approved by the ethics committee of the institutional review board.

258 ssues are discussed, and the position of the Ethics Committee of the International Xenotransplantatio

259 In the Position Paper of the Ethics Committee of the International Xenotransplantatio

260 The ethics committee of the Medical University of Vienna app

261 Ethics committee of the Medical University of Vienna, IR

262 The Ethics Committee of The Transplantation Society convened

263 93_17 B, Ethics committee of the University Hospital Erlangen-Nur

264 s This prospective study was approved by the ethics committee of the University Hospital of Munster (

265 ve data evaluation was approved by the local ethics committee of the University of Heidelberg (ethics

266 pproved by the institutional review board or ethics committees of all participating institutions, and

267 mendations approved by consensus of the full Ethics Committees of American College of Critical Care M

268 In 2014, the Cancer Prevention and Ethics Committees of ASCO commissioned another update to

269 ective study was approved by the independent ethics committees of Kanton Bern and Kanton Zurich, and

270 The study was approved by the human research ethics committees of the participating hospitals, and in

271 Retrospective registration with local ethics committee on 21 March 2019.

272 This study was approved by the local ethics committees on human studies, and written informed

273 ought that the Association should develop an ethics committee or consultation service, 55% thought it

274 pants, patients, sponsors, funders, research ethics committees or institutional review boards, peer r

275 r/director of each hospital's adult clinical ethics committee, or a suitable alternate representative

276 based cohort study was approved by a medical ethics committee overseen by the national government, an

277 sed cohort study was approved by a dedicated ethics committee overseen by the national government, an

278 this debate, the Cancer and Leukemia Group B Ethics Committee proposes guidelines for clinical trials

279 st interim analysis, the Data Monitoring and Ethics Committee recommended closure of the vosaroxin-co

280 per group); however, the data monitoring and ethics committee recommended halting the trial before fu

281 nd monitoring of clinical trials by research ethics committees (RECs).

282 2004-000991-15; Multicentre Research Ethics Committee Ref No.

283 nally, journals, funders, sponsors, research ethics committees, regulators, and legislators should en

284 e research was approved by the institutional ethics committee review board, and the volunteers provid

285 ed by the Griffith University Human Research Ethics Committee, the Stanford University Panel on Human

286 Yet researchers, funding agencies, ethics committees, the pharmaceutical industry, medical

287 Because the Ethics Committee thought the ethical and legal implicati

288 The research ethics committee waived the requirement for informed con

289 As a result, a research ethics committee was established at three hospitals in E

290 After approval from the Human Research Ethics Committee was obtained, we recruited potential re

291 Approval of the local Ethics Committee was obtained.

292 18), the input of the courts or the hospital ethics committee was obtained.

293 dy was approved by the University's research ethics committee, which conforms to the declaration of H

294 pants has allowed the creation of a national ethics committee, which serves as an entity to establish

295 ctive case-control study was approved by the ethics committee, which waived the need for patient cons

296 tained by the Southern Health Human Research Ethics Committee, which waived the requirement for infor

297 e, if clinically appropriate, (5) a Research Ethics Committee with specific transplantation expertise

298 The study protocol was approved by the local ethics committee; written informed consent was obtained.

299 This study was approved by the local ethics committee; written informed consent was obtained.

300 of the same age from 2014 to 2019 (Cantonal Ethics Committee Zurich registry number: KEK-ZH-2017-013