Clinical Trials Registration and Results Information Submission (US Department of Health and Human Services Regulation) (HHS) (2018 Edition) - The Law Library - Libros - Createspace Independent Publishing Platf - 9781729689608 - 7 de noviembre de 2018
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Clinical Trials Registration and Results Information Submission (US Department of Health and Human Services Regulation) (HHS) (2018 Edition)

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Clinical Trials Registration and Results Information Submission (US Department of Health and Human Services Regulation) (HHS) (2018 Edition) The Law Library presents the complete text of the Clinical Trials Registration and Results Information Submission (US Department of Health and Human Services Regulation) (HHS) (2018 Edition). Updated as of May 29, 2018 This final rule details the requirements for submitting registration and summary results information, including adverse event information, for specified clinical trials of drug products (including biological products) and device products and for pediatric postmarket surveillances of a device product to ClinicalTrials.gov, the clinical trial registry and results data bank operated by the National Library of Medicine (NLM) of the National Institutes of Health (NIH). This rule provides for the expanded registry and results data bank specified in Title VIII of the Food and Drug Administration Amendments Act of 2007 (FDAAA) to help patients find trials for which they might be eligible, enhance the design of clinical trials and prevent duplication of unsuccessful or unsafe trials, improve the evidence base that informs clinical care, increase the efficiency of drug and device development processes, improve clinical research practice, and build public trust in clinical research. The requirements apply to the responsible party (meaning the sponsor or designated principal investigator) for certain clinical trials of drug products (including biological products) and device products that are regulated by the Food and Drug Administration (FDA) and for pediatric postmarket surveillances of a device product that are ordered by FDA. This book contains: - The complete text of the Clinical Trials Registration and Results Information Submission (US Department of Health and Human Services Regulation) (HHS) (2018 Edition) - A table of contents with the page number of each section

Medios de comunicación Libros     Paperback Book   (Libro con tapa blanda y lomo encolado)
Publicado 7 de noviembre de 2018
ISBN13 9781729689608
Editores Createspace Independent Publishing Platf
Páginas 332
Dimensiones 178 × 254 × 18 mm   ·   576 g
Lengua Inglés  

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