Search results for " guidance" in Articles / App Notes

Article 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…

Article 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…

Article 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…

Article 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of a biosimilar molecule is one of the starting points in determining similarity to the originator medicine, with the draft guidance from FDA implying that a biosimi…

Article 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…

Article 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, …

Show All Results

Previous Page