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White Papers
Title
Author
Date
Implementing PAT and QbD? Real-time Particle Size Measurement for the Pharmaceutical Industry
03/09/2009
Performance Breakthroughs Are the Result of Human Choices, Not Technological Wizardry
ASQ
02/25/2009
FDA Regulations and Auditing Practices for Software Suppliers at a Pharmaceutical Manufacturer
ASQ
02/25/2009
Automated Inspection: Manufacturing Quality Analysis
ASQ
02/25/2009
“Thin LIMS” IT Implementation Strategy for cGMP Quality Informatics
11/14/2008
GAO: FDA Lacks “Clear and Effective Processes” for Postmarket Safety
GAO
10/27/2008
Complimentary Reports: Pharmaceutical Domain Management and Protecting Pharmaceutical Brands
MarkMonitor
10/08/2008
How New Technologies Can Improve Compliance in Pharmaceutical and Biotech Manufacturing
Justin Neway, Aegis Analytical
08/12/2008
Achieving Manufacturing Process Excellence with Quality by Design, Design Space Development, Design for Manufacturing and PAT
Aegis Analytical
08/11/2008
Felix Franks on Critical-to-Quality Process Parameters for Lyophilization
Felix Franks
03/12/2008
A Perspective on Standards
Rockwell Automation
12/17/2007
Pharmaceutical Brandjacking Index
MarkMonitor
10/05/2007
Sampling and Dispersion - The Keys to Accurate Particle Size Analysis in Pharmaceutical Materials
Malvern Instruments
09/21/2007
Residual Solvents by Teledyne Tekmar HT3 Headspace Autosampler and GCMS
Teledyne Tekmar
09/21/2007
Official File : Novartis Complaint
07/27/2007
A Guide to the GMP Requirements of PS 9000 : 2001 Pharmaceutical Packaging Materials
The Institute of Quality Assurance
07/16/2007
Environmental Testing : Deciphering Compliance Requirements for Pharmaceutical and Medical Device Manufacturers
Microtest Laboratories
07/10/2007
Aramark: Testing of Flame-Resistant Garments for Use in the Cleanroom
Mike Rataj
06/18/2007
Draft Guidance : Bioequivalence Recommendations for Specific Products
Food & Drug Administration
06/04/2007
Supply Risk Increasing While the Market Stands Still
Aberdeen Group
05/21/2007
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