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Research ethics committees: agents of research policy?

Hemminki E.

Health Res Policy Syst. 2005 Oct 4;3:6.PMID: 16202153 [PubMed]Related articlesFree article

[Reorganization of the procedures and the tasks of the responsible ethics committees after the 12th AMG amendment. Concepts of the permanent working group of the medical ethics committees in Germany]

Wessler I, Burger R, Doppelfeld E.

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Evaluation of clinical trials by Ethics Committees in Germany: experience of applicants with the review of requests for opinion of the Ethics Committees - results of a survey among members of the German Association of Research-Based Pharmaceutical Companies (VFA).

Russ H, Busta S, Riedel A, Zöllner G, Jost B.

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Research ethics committees in Europe: trials and tribulations.

Druml C, Wolzt M, Pleiner J, Singer EA.

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[The 12th amendment to the German Drug Law. Chances and obstacles for investigator-initiated clinical trials]

Dreier G, Marx C, Schmoor C, Maier-Lenz H.

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Harmonisation of ethics committees' practice in 10 European countries.

Hernandez R, Cooney M, Dualé C, Gálvez M, Gaynor S, Kardos G, Kubiak C, Mihaylov S, Pleiner J, Ruberto G, Sanz N, Skoog M, Souri P, Stiller CO, Strenge-Hesse A, Vas A, Winter D, Carné X.

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Conflicts of interest in research involving human beings.

Greco D, Diniz NM.

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Procedures and methods of benefit assessments for medicines in Germany.

Bekkering GE, Kleijnen J.

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Establishing pan-European clinical trials: regulatory compliance and other practical considerations.

Grienenberger A.

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Clinical governance and research ethics as barriers to UK low-risk population-based health research?

van Teijlingen ER, Douglas F, Torrance N.

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[Harmonisation of regulatory requirements for clinical trials on medicinal products for human use in the Directive 2001/20/EC and complementary guidance. Implementation of the 12th Law Amending the German Drug Law]

Geisler I, Hofmann HP, Nickel L.

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Ethics committees and achievement of good clinical practice.

Glasa J, Holomán J, Klepanec J, Soltés L.

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Research Ethics Committees: can they contribute to the improvement of clinical research in Europe?

Liberati A.

J Ambul Care Manage. 2004 Apr-Jun;27(2):154-65.PMID: 15069994 [PubMed - indexed for MEDLINE]Related articles

New governance arrangements for research ethics committees: is facilitating research achieved at the cost of participants' interest.

Cave E, Holm S.

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Research governance: panacea or problem?

Samanta A, Samanta J.

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European Union. Ethical considerations for clinical trials on medicinal products conducted with the paediatric population.

[No authors listed]

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[The origin of informed consent]

Mallardi V.

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Regulation of clinical research and bioethics in Portugal.

Carvalho FL.

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[Clinical trials in Germany and in the EU in the new legislative environment. An analysis from the industry's point of view]

Heidenreich K, Möritz A, Löffler H, Oberle-Rolle B.

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Professional ethics: an overview from health research ethics point of view.

Nyika A.

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