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Bioethics|January 5, 2002
Informed consent, exploitation and whether it is possible to conduct human subjects research without either oneD WendlerAnatomischer Anzeiger|January 1, 1980
[Cyclophosphamide-induced pathohistological events in the fetal rat (author's transl)]D WendlerKennedy Institute of Ethics Journal|October 20, 2001
When should "riskier" subjects be excluded from research participation?Dave WendlerTheoretical Medicine and Bioethics|March 15, 2011
What we worry about when we worry about the ethics of clinical researchDavid WendlerArchives of Toxicology. Supplement. = Archiv Fur Toxikologie. Supplement|January 1, 1980
The state and future requirements of teratogenic testingD WendlerFolia Phoniatrica Et Logopaedica : Official Organ of the International Association of Logopedics and Phoniatrics (IALP)|November 22, 2008
Singing and science. Invited lecture at the 7th Pan-European voice conference (PEVOC7), Groningen, August 28 to September 1, 2007Juergen WendlerClinical Trials (London, England)|August 19, 2020
When and how to include vulnerable subjects in clinical trialsDavid WendlerGeburtshilfe Und Frauenheilkunde|February 1, 1990
[Incidence of human papillomavirus types 31, 33 and 35 in cervix intra-epithelial neoplasms]D WendlerThe Hastings Center Report|December 27, 2018
Locating the Source(s) of the Social Value Requirement(s)David WendlerKennedy Institute of Ethics Journal|July 30, 2004
Risk standards for pediatric research: rethinking the Grimes rulingDavid WendlerPageof 369