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Common Issues in Ethical Review of Research: A Perspective from Pakistan, Slides of Biotechnology

Common issues in ethical review of research from a pakistani perspective, focusing on training deficiencies, misinformed consent, conflicting interests, and the review process in pakistan. The document also provides recommendations for enhancing irbs' capacity and improving informed consent processes.

Typology: Slides

2012/2013

Uploaded on 02/06/2013

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Download Common Issues in Ethical Review of Research: A Perspective from Pakistan and more Slides Biotechnology in PDF only on Docsity! Common issues in ethical review of research: a Pakistani perspective Docsity.com Outline ā€¢ Research scenario in Pakistan ā€¢ Issues ļ Training deficiencies ļ Misinformed consent ļConflicting interests ļ Review process Docsity.com INTERNATIONAL IRBS FOR PAKISTAN (12) [NEW SEARCH Find Institutional Review Boards in table below and click corresponding Detail link to view details: ituti Navigate tei a Eaasnay Boards IRB Number Institutional Review Board City IRBOO001234 AGA Khan U IRB #1 Karachi Detail IRBOOOO1794 National Ctr Excellence in Molecular Biology U IRB #1 Lahore Detail IRBOOOOZ208 Health Oriented Prev Education (HOPE) IRB #1 Karachi Detail TRBOOOOZ510 Nai Zindagi IRB #1 Islamabad Detail IRBOOOO2993 ARI Rech CELL IRB #1 Islamabad Detail TRBOOOO3084 Sindh AIDS Control Program IRB #1 Karachi Detail IRBOOOO3157 Bridge IRB #1 Karachi Detail IRBOOGO3532 Quaid-I-azam U IRB #1 - Biomedical Islamabad Detail IRBOOGOS148 Interactive Research and Development. IRB #1 Karachi Detail IRBOOGOSZ81 School of Biological Sciences IRB #1 Lahore Detail IREQOOOS335 Human Development Research Foundation IRB #1 Islamabad Detail IRBOOOOSS56 Faculty of Biotechnology Ā¢Informatics IRB #1 Quetta Detail ww.hhs.gov/ohrp/humansubjects/assurance/renwirb.htm Docsity.com Issues Docsity.com Training deficiencies ā€¢ Undergraduate and postgraduate ā€¢ Lack of opportunities ā€¢ Dearth of capacity ā€¢ Over-training versus non exposure Docsity.com Misinformed consent ā€¢ Confusion between research and clinical care ā€¢ ā€œRandomizationā€, ā€œplaceboā€ or ā€œcontrolā€, ā€œdouble blindā€ translated literally ļ¶ā€œPlaceboā€ translated as ā€œineffective drugā€ Docsity.com Conflicting Interests ā€¢ Incentives for researchers ā€¢ Incentives for recruitment Docsity.com Conflicting interests: incentives for researchers ā€¢ Level of compensation for Principal Investigator ā€¢ Reward for recruitment of subjects for research officers What is the role of IRBā€™s in this? Docsity.com Recommendations ā€¢ Enhance IRBsā€™ capacity to review beyond guidelines ā€¢ Probe potential conflict of interest areas ā€¢ Informed consent should be contextual ā€“ written for subjects who can read and write ā€“ verbal and witnessed for subjects who cannot read and write Docsity.com Recommendations contd. ā€“ audio-visual materials, brochures etc. to communicate complex information ā€“ translations should capture concept ā€¢ Lack of adequate health care infrastructure requires IRBs in developing world to be more vigilant Docsity.com
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