Rockville, MD, U.S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research | Center for Biologics Evaluation and Research, 1999
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The event Rockville, MD, U.S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research | Center for Biologics Evaluation and Research, 1999 represents a publication, printing, distribution, issue, release or production of resources found in Biddle Law Library - University of Pennsylvania Law School.
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Rockville, MD, U.S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research | Center for Biologics Evaluation and Research, 1999
Resource Information
The event Rockville, MD, U.S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research | Center for Biologics Evaluation and Research, 1999 represents a publication, printing, distribution, issue, release or production of resources found in Biddle Law Library - University of Pennsylvania Law School.
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- Rockville, MD, U.S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research | Center for Biologics Evaluation and Research, 1999
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- 1999
6 Items that share the ProviderEvent Rockville, MD, U.S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research | Center for Biologics Evaluation and Research, 1999
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Context of Rockville, MD, U.S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research | Center for Biologics Evaluation and Research, 1999Publication of
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- Guidance for industry : Q6B specifications : test procedures and acceptance criteria for biotechnological /biological products
- Guidance for industry : accelerated approval products, submission of promotional materials
- Guidance for industry : container closure systems for packaging human drugs and biologics
- Guidance for industry : population pharmacokinetics
- Guidance for industry : providing regulatory submissions in electronic format, general considerations
- Guidance for industry : qualifying for pediatric exclusivity under section 505A of the Federal Food, Drug, and Cosmetic Act
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<div class="citation" vocab="http://schema.org/"><i class="fa fa-external-link-square fa-fw"></i> Data from <span resource="http://link.law.upenn.edu/resource/sKVRdA_v38s/" typeof="PublicationEvent http://bibfra.me/vocab/lite/ProviderEvent"><span property="name http://bibfra.me/vocab/lite/label"><a href="http://link.law.upenn.edu/resource/sKVRdA_v38s/">Rockville, MD, U.S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research | Center for Biologics Evaluation and Research, 1999</a></span> - <span property="potentialAction" typeOf="OrganizeAction"><span property="agent" typeof="LibrarySystem http://library.link/vocab/LibrarySystem" resource="http://link.law.upenn.edu/"><span property="name http://bibfra.me/vocab/lite/label"><a property="url" href="http://link.law.upenn.edu/">Biddle Law Library - University of Pennsylvania Law School</a></span></span></span></span></div>