Mixing , Diluting, or Repackaging Biological Products Outside the Scope of An Approved Biologics License Application

First Page		Document Content
Pharmaceutical sciences Biologic License Application Center for Biologics Evaluation and Research Biologic Federal Food Drug and Cosmetic Act Center for Drug Evaluation and Research Abbreviated New Drug Application Good manufacturing practice Biosimilar Food and Drug Administration Medicine Health		Mixing , Diluting, or Repackaging Biological Products Outside the Scope of An Approved Biologics License Application Add to Reading List Source URL: www.fda.gov Download Document from Source Website File Size: 227,08 KB Share Document on Facebook

	Federal Register / Vol. 83, NoFriday, March 16, Proposed Rules Food and Drug Administration 21 CFR Part 1130 DocID: 1xVJS - View Document
	Federal Department of Home Affairs FDHA Federal Food Safety and Veterinary Office FSVO Animal Health July 2018 DocID: 1xUDM - View Document
	Federal Department of Home Affairs FDHA Federal Food Safety and Veterinary Office FSVO International Affairs Re-import of CITES goods in Switzerland DocID: 1xU2i - View Document
	Federal Department of Home Affairs FDHA Federal Food Safety and Veterinary Office FSVO Animal Health Animal health statistics for 2017 The obligation to report diseases and suspected disease symptoms is laid down in Arti DocID: 1xTRC - View Document
	From the Field to the Farm Bill: Can Federal Policy Changes Help Grow Local Food Systems? March 2011 Kristen Loria, Cornell University, Class ofStrong local and regional food systems are essential DocID: 1uY95 - View Document