Title
|
Author
|
Date
|
| Ensuring Quality & Regulatory Compliance When Collaborating with a Service Provider |
DPT Laboratories |
09/05/2012 |
| |
| Evaluating Library Databases for Microbial Identification: Critical Aspects and Recommendations |
|
07/07/2011 |
| |
| Reducing Airborne Contaminants with Polymeric Floor Coverings |
|
07/07/2011 |
| |
| Competitiveness and Regulation: The FDA and the Future of America's Biomedical Industry |
|
02/22/2011 |
| |
| Compliance, Risk and Cost of Ownership Comparisons for Pharmaceutical Continuous Monitoring: Wired, Wireless and Standalone Monitoring Systems |
Ken Appel, Manager Regulated Markets, Veriteq, a Vaisala company |
02/03/2011 |
| |
| How to Respond to (and Avoid) FDA 483s |
Veriteq, a Vaisala company |
01/24/2011 |
| |
| Joining Forces: Bringing Pharma Supply Chain Management and Supply Quality Management Together |
|
08/03/2010 |
| |
| FDA Transparency Initiative: Opening FDA's 'Black Box' |
Afia K. Asamoah, published by FDLI |
02/23/2010 |
| |
| Enhancing Collaboration with the FDA Through MedWatch Plus |
ETQ Inc. |
02/08/2010 |
| |
| Accounting for Risk in Your Asset Management Strategy |
Life Cycle Engineering |
09/23/2009 |
| |
| Integrating Good Manufacturing Practices During the Transition from Clinical Trials to Commerical Manufacturing |
CDC Software |
06/11/2009 |
| |
| Current Trends in GMP Warning Letters |
Hogan & Hartson LLP |
05/22/2009 |
| |
| Imperfect Harmony: Life Sciences Companies Must Partner to Thrive |
IBM |
03/16/2009 |
| |
| “Thin LIMS” IT Implementation Strategy for cGMP Quality Informatics |
|
11/14/2008 |
| |
| 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 |
| |
| A Perspective on Standards: A Tool for Global Competitive Survival in an Increasingly Complex Regulatory World |
Rockwell Automation |
02/22/2008 |
| |
| Amendment to the cGMP Regulations for Finished Pharmaceuticals |
FDA |
12/07/2007 |
| |
| Official File : Novartis Complaint |
|
07/27/2007 |
| |
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