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A CTSA One Health Alliance guidance on institutional review of veterinary clinical studies.
Moore, S A; O'Kell, A; Borghese, H; Garabed, R; O'Meara, H; Baneux, P.
Afiliação
  • Moore SA; Department of Veterinary Clinical Sciences, The Ohio State University College of Veterinary Medicine, 601 Vernon L Tharp St, Columbus, OH, 43210, USA. moore.2204@osu.edu.
  • O'Kell A; Department of Small Animal Clinical Sciences, University of Florida College of Veterinary Medicine, Gainesville, USA.
  • Borghese H; The Ohio State University College of Veterinary Medicine, Blue Buffalo Veterinary Clinical Trials Office, Columbus, USA.
  • Garabed R; Department of Veterinary Preventive Medicine, The Ohio State University College of Veterinary Medicine, Columbus, USA.
  • O'Meara H; The Ohio State University, Office of Responsible Research Practices, Columbus, USA.
  • Baneux P; Cornell University, Attending veterinarian, Director Center for Animal Resources and Education, Ithaca, USA.
BMC Vet Res ; 17(1): 83, 2021 Feb 17.
Article em En | MEDLINE | ID: mdl-33596904
Harmonized institutional processes and reviewer training are vital to maintain integrity and ethical rigor of the veterinary clinical research pipeline and are a prerequisite to future work that might establish centralized or single-site ethical and regulatory review to ease initiation of multi-center studies. Funded by a CTSA One Health Alliance (COHA) pilot award, a diverse working group of veterinary clinicians and institutional representatives was convened in February 2020 to develop a guidance document detailing broadly agreed upon practices for ethical review and approval of veterinary clinical studies conducted in the United States.The working group defined key areas of need for consensus, developed a set of associated guidelines, and circulated these for review by COHA's fifteen member institutions. Six focus areas were identified by the working group and included vital items of protocol review, composition of the review committee, post-approval monitoring and adverse event reporting, consideration of special circumstances such as satellite sites and the use of healthy veterinary subjects in research, and the informed consent process.This document outlines a broadly agreed-upon framework through which to approach vital items associated with veterinary clinical study protocol review and approval. These approaches represent current best practice in the review and approval of veterinary clinical studies, and can serve as a guidance for veterinary clinician-scientists and regulatory experts, to ensure robust and ethically conducted studies that can contribute to the advancement of both animal and human health.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pesquisa / Medicina Veterinária / Bem-Estar do Animal Tipo de estudo: Guideline / Prognostic_studies Aspecto: Ethics Limite: Animals País/Região como assunto: America do norte Idioma: En Revista: BMC Vet Res Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pesquisa / Medicina Veterinária / Bem-Estar do Animal Tipo de estudo: Guideline / Prognostic_studies Aspecto: Ethics Limite: Animals País/Região como assunto: America do norte Idioma: En Revista: BMC Vet Res Ano de publicação: 2021 Tipo de documento: Article