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Ethics committee (European Union)

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198: 62:(EU) envisioned a harmonisation of research ethics committees (RECs) across Europe, including the time taken to assess a trial proposal and the kinds of issues a committee should take into account. 47:, the suitability of the investigators involved in the trial and the adequacy of facilities, and on the methods and documents to be used to inform trial subjects and obtain their 156:
A Hedgecoe, F Carvalho, P Lobmayer and F Raka, Research ethics committees in Europe: implementing the directive, respecting diversity, Journal of Medical Ethics 2006;32:483-486.
39:, consisting of healthcare professionals and non-medical members, whose responsibility is to protect the rights, safety and well being of human subjects involved in a 17: 239: 145: 183: 268: 178: 258: 123: 263: 172: 232: 213: 151: 166: 43:
and to provide public assurance of that protection, by, among other things, expressing an opinion on the
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A Medical Research Ethics Committee (MREC) in the Netherlands.
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A Research Ethics Committee (REC) in the United Kingdom
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A Comités de Protection des Personnes (CPP) in France.
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Local terms for a European ethics committee include:
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New Zealand Health and Disability Ethics Committees
35:, is an independent body in a member state of the 250: 148:of the European Parliament and of the Council. 233: 152:Implementing texts for Directive 2001/20/EC 240: 226: 14: 251: 184:Research Ethics Committees - Documents 75:An Ethical Vetting Board in Sweden - ( 192: 24: 25: 280: 160: 18:Ethics Committee (European Union) 196: 167:National Research Ethics Service 124:Regulation of therapeutic goods 13: 1: 269:Philosophy organization stubs 139: 212:. You can help Knowledge by 7: 208:-related organization is a 169:(NRES (Formerly COREC), UK) 86: 10: 285: 259:European clinical research 191: 173:National ethics committees 118:Institutional Review Board 129:European Medicines Agency 56:Clinical Trials Directive 134:Investigator's brochure 45:clinical trial protocol 204:This article about a 264:Ethics organizations 146:Directive 2001/20/EC 108:Directive 2005/28/EC 77:Etikprövningsnämnden 33:Directive 2001/20/EC 221: 220: 16:(Redirected from 276: 242: 235: 228: 200: 193: 113:Qualified Person 98:Ethics committee 49:informed consent 29:ethics committee 21: 284: 283: 279: 278: 277: 275: 274: 273: 249: 248: 247: 246: 189: 163: 142: 93:Research ethics 89: 31:, according to 23: 22: 15: 12: 11: 5: 282: 272: 271: 266: 261: 245: 244: 237: 230: 222: 219: 218: 201: 187: 186: 181: 176: 170: 162: 161:External links 159: 158: 157: 154: 149: 141: 138: 137: 136: 131: 126: 121: 115: 110: 105: 100: 95: 88: 85: 84: 83: 80: 73: 70: 60:European Union 41:clinical trial 37:European Union 9: 6: 4: 3: 2: 281: 270: 267: 265: 262: 260: 257: 256: 254: 243: 238: 236: 231: 229: 224: 223: 217: 215: 211: 207: 202: 199: 195: 194: 190: 185: 182: 180: 177: 174: 171: 168: 165: 164: 155: 153: 150: 147: 144: 143: 135: 132: 130: 127: 125: 122: 119: 116: 114: 111: 109: 106: 104: 101: 99: 96: 94: 91: 90: 81: 78: 74: 71: 68: 67: 66: 63: 61: 57: 52: 50: 46: 42: 38: 34: 30: 19: 214:expanding it 203: 188: 76: 64: 53: 28: 26: 79:in Swedish) 253:Categories 206:philosophy 140:References 54:With the 103:EudraLex 87:See also 58:, the 120:(IRB) 210:stub 175:(EU) 27:The 255:: 51:. 241:e 234:t 227:v 216:. 20:)

Index

Ethics Committee (European Union)
Directive 2001/20/EC
European Union
clinical trial
clinical trial protocol
informed consent
Clinical Trials Directive
European Union
Research ethics
Ethics committee
EudraLex
Directive 2005/28/EC
Qualified Person
Institutional Review Board
Regulation of therapeutic goods
European Medicines Agency
Investigator's brochure
Directive 2001/20/EC
Implementing texts for Directive 2001/20/EC
National Research Ethics Service
National ethics committees
New Zealand Health and Disability Ethics Committees
Research Ethics Committees - Documents
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philosophy
stub
expanding it
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