Checklist and Guide to Patient Consent

Patient consent is an essential basis for the legally compliant collection, processing, and use of pseudonymized patient data in studies and research projects. This results in high demands on the information content and the clear documentation of the patient's will in relation to the respective project. Medical, ethical, and data protection regulations must be observed when formulating patient information and consent forms.

The third volume of the TMF publication series is a reference work that enables users to create patient information and consent forms based on relevant, documented, and annotated sources to create patient information and consent forms that meet regulatory demands.

In addition to the requirements for creating a patient information and consent form for adults capable of giving consent, it also contains the special requirements that must be taken into account when processing biomaterials in the context of specific research projects or when setting up biomaterial banks.

U. Harnischmacher | P. Ihle | B. Berger | J. W. Goebel | J. Scheller:
Checkliste und Leitfaden zur Patienteneinwilligung
Grundlagen und Anleitung für die klinische Forschung

1st edition, 176 pages, December 2006
€ 44.95 [D], ISBN 978-3-939069-25-6

Copyright and license conditions for this product

Please note the copyright conditions printed in the book.