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DRAP Draft Guidance on Clinical Research: Responsibilities
The new article describes in detail the key responsibilities of the parties involved in clinical research.
The new article describes in detail the key responsibilities of the parties involved in clinical research.
The article highlights the aspects related to the rights and responsibilities of Institutional Review Boards in the context of informed consent. Table of Contents The Food and Drug Administration (FDA or the Agency), the US regulating authority in the sphere...
The FDA and Human Health Services (HHS) has recently finalized guidance on the written procedures of institutional review boards (IRB). IRBs are dedicated to supervising and approving studies that involve humans, while also maintaining fair and safe treatment of those...