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Subject
Department
Industry
Date
Generating High Performance: Beyond Technical Abilities
Training/Learning & Development
Other
16 Mar 2010
QA Oversight of Vendor Management
Quality
Pharmaceuticals
17 Mar 2010
Electronic Informed Consent: Putting the Pieces Together for Implementation
Clinical
Pharmaceuticals
18 Mar 2010
Periodic Safety Update Reports: Be Compliant and Cost Effective
Clinical
Pharmaceuticals
23 Mar 2010
Comparative Costs of Clinical Development in CEE and Other Regions
Clinical
Pharmaceuticals
24 Mar 2010
Is Your Product Development Cycle Ready for IEC 60601-1 3rd Edition?
Engineering/R&D
Medical Devices
25 Mar 2010
Good Auditing Practices for EU Notified Body Audits
Regulatory
Medical Devices
30 Mar 2010
Video Production and Localization for eLearning
Marketing/Corporate Communication
Other
6 Apr 2010
Building Better Clinician Relationships
Regulatory
Pharmaceuticals
8 Apr 2010
Medical Device Vigilance Planning under the Revised MDD
Regulatory
Medical Devices
13 Apr 2010
1
2
Popular Events
Adaptive/Novel Designs in Oncology: Overview & Issues
Dr. John Constant, PRA International
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Dr. John Powers, George Washington University School of Medicine & Dr. Carl Kraus, PRA International
An Overview of EMEA & Centralized Procedure
Dr. Ulrich Granzer, Granzer Regulatory Consulting
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