Search results for " guidance" in Articles / App Notes
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				FDA Seeks Metrics to Define Drug Quality
								Despite a decade of encouragement and guidance from FDA, manufacturers have failed to adopt a “continuous improvement model,” according to Janet Woodcock, director of the Center for Drug Evaluation an…								
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				Operational Excellence: More Than Just Process Improvement
								…ions staff, there to help assure quality and compliance, but also to help address issues and provide guidance to help up-skill shop floor personnel in their understanding and performance of cGMP/comp…								
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				Essentials in Establishing and Using Design Space
								FDA, Guidance for Industry, Process Validation: General Principles 
	
	and Practices (2011). 
	
	3. S. Chatterjee, “Design Space Considerations,” FDA, AAPS Annual Meeting, October 14, 2012, Chicago, O…								
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				Elucidating Biosimilars Characterization
								Quintiles: The amino-acid sequence of a biosimilar molecule is one of the starting points in determining similarity to the originator medicine, with the draft guidance from FDA implying that a biosimi…								
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				PDA's Technical Report for Biotech Cleaning Validation
								The report provides a single-source overview for biotechnology manufacturers and complements existing guidance and reference documents. It builds on and updates previous PDA publications, including th…								
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				Addressing the Challenges in Downstream Processing Today and Tomorrow
								FDA, Guidance for Industry: Evaluation of Combination Vaccines for Preventable Diseases: Production, Testing and Clinical Studies (Rockville, MD, April 1997). 
	
	42. G.T. Jennings and M.F. Bachmann, …