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Monitoring clinical research: an obligation unfulfilled.

Monitoring clinical research: an obligation unfulfilled.

http://www.wikidata.org/entity/Q34279586

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Monitoring and oversight in critical care research The structure and function of research ethics committees in Africa: a case study.A cluster randomised trial of a telephone-based intervention for parents to increase fruit and vegetable consumption in their 3- to 5-year-old children: study protocol Continuing review of research approved by Canadian research ethics boards Methodological quality and reporting of ethical requirements in phase III cancer trials Competing commitments in psychiatric research: an examination of psychiatric researchers' perspectives Views and experiences of IRBs concerning research integrity.Are research ethics committees behaving unethically? Some suggestions for improving performance and accountability.Are institutional review boards prepared for active continuing review?Monitoring clinical research: report of one hospital's experience.Continuing review of ethics in clinical trials: a surveillance study in Iran

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P2860

Monitoring clinical research: an obligation unfulfilled.

http://www.wikidata.org/entity/Q34279586

description

1995 nî lūn-bûn

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1995 թուականի Յունիսին հրատարակուած գիտական յօդուած

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1995 թվականի հունիսին հրատարակված գիտական հոդված

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1995年の論文

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1995年学术文章

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1995年学术文章

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1995年学术文章

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1995年学术文章

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1995年学术文章

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1995年學術文章

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name

Monitoring clinical research: an obligation unfulfilled.

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Monitoring clinical research: an obligation unfulfilled.

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Monitoring clinical research: an obligation unfulfilled.

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Monitoring clinical research: an obligation unfulfilled.

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Monitoring clinical research: an obligation unfulfilled.

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Monitoring clinical research: an obligation unfulfilled.

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Monitoring clinical research: an obligation unfulfilled.

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Monitoring clinical research: an obligation unfulfilled.

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Monitoring clinical research: an obligation unfulfilled.

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Canadian Medical Association Journal

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Monitoring clinical research: an obligation unfulfilled.

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Fuks A

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Glass KC

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Shapiro S

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Skrutkowska M

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Weijer C

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P2860

Quality control of dietary data collection in the CARDIA study.

Data integrity.

A case of data alteration in the Multiple Risk Factor Intervention Trial (MRFIT). The MRFIT Research Group.

Detecting fabrication of data in a multicenter collaborative animal study.

The role of data audits in detecting scientific misconduct. Results of the FDA program.

An assessment of institutional review committees in human experimentation.

Equipoise and the ethics of clinical research.

Comprehension of informed consent for research: issues and directions for future study.

Should IRBs monitor research more strictly?

Ethics review in Canada: highlights from a national workshop, part 1.

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scholarly article

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1338019

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