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Food and drug administration's requirements for markers

Controlled Clinical Trials, 1984
Three basic principles must be satisfied when a substance is being considered for human ingestion: The composition of the product must be consistent within certain limits over a specific period of time. It must not produce irreversible harm or unacceptable side effects.
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Perspective of the Food and Drug Administration

1990
While this chapter is primarily concerned with describing the perspective of the Food and Drug Administration (FDA) about what constitutes appropriate controlled trials of drugs in patients with epilepsy, it is impossible to fully understand the Agency’s viewpoint without some understanding of the legal and regulatory foundation of the Agency’s ...
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Food and Drug Administration (FDA)

2009
U.S. American regulatory authority responsible for investigational new drugs and for the marketing authorisation of them; → see also fda, new drug application.
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The Corporate Assault on the Food and Drug Administration

International Journal of Health Services, 1996
Current “regulatory reform” in the U.S. Congress is seeking to eliminate the Food and Drug Administration. The author discusses the forces behind this reform and traces the impact of campaign contributions from various industries opposed to FDA regulations, stock held by members of Congress in companies regulated by the FDA, and a variety of ...
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Devices and the Food and Drug Administration

Artificial Organs, 2005
Rachel S. Phillips, Steven J. Phillips
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Evolving standards of care and new challenges in the management of HER2‐positive breast cancer

Ca-A Cancer Journal for Clinicians, 2020
Ciara C O’sullivan   +2 more
exaly  

Photodynamic therapy of cancer: An update

Ca-A Cancer Journal for Clinicians, 2011
Patrizia Agostinis   +2 more
exaly  

Innovations in research and clinical care using patient‐generated health data

Ca-A Cancer Journal for Clinicians, 2020
Heather S L Jim   +2 more
exaly  

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