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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Draft Guidance : Bioequivalence Recommendations for Specific Products Food & Drug Administration 06/04/2007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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