FDA's Role in Public Health: Drug Efficacy, Safety, Quality, and Beyond - Certificate of Completion 2015-2019
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The online format was appropriate for the subject matter and I was able to access all components of the activity without difficulty.
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This activity supported achievement of each of the learning objectives.
Describe and explain the drug development and review process in the United States for new drugs, generics, over-the-counter (OTC) drugs, and biosimilars
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Outline CDER’s role in post-marketing safety surveillance for medical products
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Identify ways CDER disseminates safety information about medical products to both health care professionals and their patients
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Describe CDER initiatives and commitments for the protection of public health
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The material was organized clearly for learning to occur.
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The content learned from this activity will impact my practice.
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Does this activity promote improvement in healthcare?
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The activity was presented objectively and was free of commercial bias.
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 I would recommend this activity to others.
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Please list FDA training topics that would be of value to you.
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