SCOPUS 정보 검색 플랫폼

Volumn 35, Issue 4, 2009, Pages 613-615

Protocols in expedited review: Tackling the workload of ethics committees

Author keywords

Ethics Committee; European legislation; Expedited review; Minimal risk

Indexed keywords

JOB PERFORMANCE; MEDICAL RESEARCH; OCCUPATIONAL HAZARD; PROFESSIONAL STANDARD; REVIEW; STRUCTURED QUESTIONNAIRE; WORK EXPERIENCE; WORKLOAD;

ACADEMIC MEDICAL CENTERS; AUSTRIA; CLINICAL PROTOCOLS; ETHICS COMMITTEES; HUMANS; RISK MANAGEMENT; UNIVERSITIES; VULNERABLE POPULATIONS; WORKLOAD;

EID: 62949122351 PISSN: 03424642 EISSN: 14321238 Source Type: Journal
DOI: 10.1007/s00134-008-1343-x Document Type: Review

Times cited : (12)

References (7)

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- Vick, C.C.¹ Finan, K.R.² Kiefe, C.³ Neumayer, L.⁴ Hawn, M.T.⁵

2
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- Impact of institutional review board practice variation on observational health services research
- LA Green JC Lowery CP Kowalski L Wyszewianski 2006 Impact of institutional review board practice variation on observational health services research Health Serv Res 41 214 230
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- Green, L.A.¹ Lowery, J.C.² Kowalski, C.P.³ Wyszewianski, L.⁴

3
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- Medical education research and IRB review: An analysis and comparison of the IRB review process at six institutions
- LN Dyrbye MR Thomas AJ Mechaber 2007 Medical education research and IRB review: an analysis and comparison of the IRB review process at six institutions Acad Med 82 654 660
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- Dyrbye, L.N.¹ Thomas, M.R.² Mechaber, A.J.³

4
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- A survey of IRB process in 68 US hospitals
- E Larson T Bratts J Zwanziger P Stone 2004 A survey of IRB process in 68 US hospitals J Nurs Scholarsh 36 260 264
- (2004) J Nurs Scholarsh , vol.36 , pp. 260-264
- Larson, E.¹ Bratts, T.² Zwanziger, J.³ Stone, P.⁴

5
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- World Health Organization Accessed 01 Sept 2008
- World Health Organization (2000) Operational guidelines for Ethics Committees that review biomedical research. Available at http://www.who.int/tdr/ publications/publications/pdf/ethics.pdf. Accessed 01 Sept 2008
- (2000) Operational Guidelines for Ethics Committees That Review Biomedical Research

6
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- European Commission Accessed 01 Sept 2008
- European Commission (2006) Definition of investigational medicinal products (IMPs), definition of non investigational medicinal products (NIMPs). Available at http://ec.europa.eu/enterprise/pharmaceuticals/pharmacos/docs/ doc2006/07-2006/def-imp-2006-07-27.pdf. Accessed 01 Sept 2008
- (2006) Definition of Investigational Medicinal Products (IMPs), Definition of Non Investigational Medicinal Products (NIMPs)

7
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- Directive 2001/20/EC of the European Parliament and of the Council of 4 April 2001 on the approximation of the laws, regulations and administrative provisions of the Member States relating to the implementation of good clinical practice in the conduct of clinical trials on medicinal products for human use
- Directive 2001/20/EC of the European Parliament and of the Council of 4 April 2001 on the approximation of the laws, regulations and administrative provisions of the Member States relating to the implementation of good clinical practice in the conduct of clinical trials on medicinal products for human use (2001) J Eur Commun L 121:34-44
- (2001) J Eur Commun L , vol.121 , pp. 34-44

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.