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Subjects (1-4 of 4)
Drugs Side Effects Reporting
1
Guidance for industry addendum to E2C clinical safety data management : periodic safety update repo
Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research : Center for Biologics Evaluation and Research, [2004] 2004
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Axe Federal Documents Online
HE 20.4702:D 26/4
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2
Guidance for industry pharmacovigilance of veterinary medicinal products : management of periodical
Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Veterinary Medicine, [2001] 2001
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Axe Federal Documents Online
HE 20.4402:P 49/2
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3
Methods of therapeutic drug monitoring including pharmacogenetics
Amsterdam, Netherlands : Elsevier, [2020] 2020
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Axe Elsevier ScienceDirect Ebook
Electronic Book
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4
Post-approval safety data management definitions and standards for expedited reporting.
[Rockville, Md.? : U.S. Dept. of Health and Human Services, Food and Drug Administration, 2003] 2003
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Axe Federal Documents Online
HE 20.4002:SA 1/8
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