![Clinical research / Pharmaceutical industry / Food and Drug Administration / Design of experiments / Institutional review board / Clinical trial / Public Responsibility in Medicine and Research / Investigational device exemption / Office for Human Research Protections / Clinical investigator / Human subject research / Covered clinical study Clinical research / Pharmaceutical industry / Food and Drug Administration / Design of experiments / Institutional review board / Clinical trial / Public Responsibility in Medicine and Research / Investigational device exemption / Office for Human Research Protections / Clinical investigator / Human subject research / Covered clinical study](https://www.pdfsearch.io/img/5cb7d96bdeed349c327dfaf5e231bdb0.jpg) Date: 2014-01-30 11:37:27Clinical research Pharmaceutical industry Food and Drug Administration Design of experiments Institutional review board Clinical trial Public Responsibility in Medicine and Research Investigational device exemption Office for Human Research Protections Clinical investigator Human subject research Covered clinical study | | § CFR Ch. I (4–1–12 Edition) (3) Requesting that the applicant conduct additional independent studiesAdd to Reading ListSource URL: publicfiles.jaeb.orgDownload Document from Source Website File Size: 198,14 KBShare Document on Facebook
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