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Accountability in Research
Ethics, Integrity and Policy
Volume 21, 2014 - Issue 5
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Policies and Quality Assurance

Overcoming Language Barriers in the Informed Consent Process: Regulatory and Compliance Issues with the Use of the “Short Form”

Pramod M. LadChildren’s Hospital Los Angeles, Los Angeles, California, USACorrespondence[email protected]
, Ph.D. , C.I.P. &
Rebecca DahlChildren’s Hospital Los Angeles, Los Angeles, California, USA
, Ph.D. , C.I.P.
Pages 315-320 | Published online: 13 Mar 2014

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Pramod M. Lad & Rebecca Dahl. (2015) Defining the Research Category in Pediatric Phase I Oncology Trials. Accountability in Research 22:3, pages 139-147.
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Articles from other publishers (2)

X. Mona Guo, Monica K. Neuman, Andrew Vallejo, Koji Matsuo & Lynda D. Roman. (2024) An absence of translated consent forms limits oncologic clinical trial enrollment for limited English proficiency participants. Gynecologic Oncology 180, pages 86-90.
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Gianna McMillan. (2020) IRB Policies for Obtaining Informed Consent from Non‐English‐Speaking People. Ethics & Human Research 42:3, pages 21-29.
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