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Dr. Suzanne Thomas, a psychologist with her PhD in experimental psychology, discusses the important role of the Institutional Review Board (IRB) to ensure ethical and relevant research, proper clinical protocol, safety of participants, as well as informed consent for all clinical trials. She indicates common obstacles for investigators in gaining IRB approval. To conclude this podcast, Dr. Thomas points to the particularly stringent requirements of confidentiality for substance abuse research.
Right click the Download Podcast link and select "Save Target As..." to download this file to your MP3 player. Select the grey arrow or the Listen Now link to listen on your computer. Listen Now | Download Podcast (mp3)
File Size: 6.37 MB Time: 6:58 Min.
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