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Free access

Research article

First published 1998-12

Psychiatrists' Documentation of Informed Consent

Debbie Schachter, Irwin Kleinman

The Canadian Journal of Psychiatry

Retricted access

Research article

First published 1995-10

A Computerized Informed Consent Document

Ruth Fries, James Ray

Therapeutic Innovation & Regulatory Science

Free access

Research article

First published 2006-6

Psychiatrists' Documentation of Informed Consent: A Representative Survey

Debbie Schachter, Irwin Kleinman

The Canadian Journal of Psychiatry

Retricted access

Other

First published 2000-10

The Informed Consent form: Document Development and Evaluation

Mark Hochhauser

Therapeutic Innovation & Regulatory Science

Open access

Research article

First published 2021-2

Details of risk–benefit communication in informed consent documents for phase I/II trials

Hannes Kahrass, Sabine Bossert, Christopher Schürmann [...]

Clinical Trials

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Research article

First published 2012-10

Readability of Informed Consent Documents (1987–2007) for Clinical Trials: A Linguistic Analysis

K. Sand, N.L. Eik-Nes, J. H. Loge

Journal of Empirical Research on Human Research Ethics

Retricted access

Research article

First published 2025-7

Content and Readability of Informed Consent Documents Approved by Research Ethics Committees of Health Institutions in South-East Nigeria

Onyinye Chime, Emmanuel Ezeome

Journal of Empirical Research on Human Research Ethics

Retricted access

Research article

First published 2009-11

Applying a Sociolinguistic Model to the Analysis of Informed Consent Documents

José Granero-Molina, Cayetano Fernández-Sola, Gabriel Aguilera-Manrique

Nursing Ethics

Retricted access

Research article

First published 1999-11

Effectiveness of a Writing Improvement Intervention Program on the Readability of the Research Informed Consent Document

Sandra J. Philipson, Mary Anne Doyle, Charles Nightingale [...]

Journal of Investigative Medicine

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Other

First published 2004-10

The Problem of Readability of Informed Consent Documents for Clinical Trials of Investigational Drugs and Devices: United States Considerations

S. Michael Sharp

Therapeutic Innovation & Regulatory Science

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