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 Understanding Information Quality Management as a Change Programme
ITXpertpanel
[November 15, 2012 - November 15, 2012]
Computer and IT
TBA
Online Training,
Wilmington,
Delaware
[USA]
 Taking Your Brand Mobile to App or Not to App
ITXpertpanel
[November 8, 2012 - November 8, 2012]
Computer and IT
TBA
Wilmington,
Delaware
[USA]
 Bullet-Proof Closed-Loop CAPA
GlobalCompliancePanel
[October 31, 2012 - October 31, 2012]
Medical and Pharmaceuticals
»
Medical Devices
TBA
Wilmington,
Delaware
[USA]
 South Korea Navigating the Clinical Trial and Regulatory Environment
GlobalCompliancePanel
[October 31, 2012 - October 31, 2012]
Medical and Pharmaceuticals
»
Pharmaceutical Products
TBA
Wilmington,
Delaware
[USA]
 How FDA Trains its Investigators to Review CAPA and What You Should Do to Prepare
GlobalCompliancePanel
[October 30, 2012 - October 30, 2012]
Medical and Pharmaceuticals
»
Medical Devices
TBA
Wilmington,
Delaware
[USA]
 Update on Unique Device Identifier for Device Manufacturers
GlobalCompliancePanel
[October 30, 2012 - October 30, 2012]
Medical and Pharmaceuticals
»
Medical Devices
TBA
Wilmington,
Delaware
[USA]
 RAPS Approved Earn 12 RAC Points
GlobalCompliancePanel
[October 29, 2012 - October 30, 2012]
Medical and Pharmaceuticals
TBA
Mumbai,
Maharashtra
[India]
 Good Laboratory Practice Regulations Introduction and Strategies for Implementation
GlobalCompliancePanel
[October 25, 2012 - October 25, 2012]
Medical and Pharmaceuticals
»
Analytical Products
TBA
Wilmington,
Delaware
[USA]
 Medical Device Reporting
GlobalCompliancePanel
[October 25, 2012 - October 25, 2012]
Medical and Pharmaceuticals
»
Medical Devices
TBA
Wilmington,
Delaware
[USA]
 Computer Systems Used in Clinical Trials
GlobalCompliancePanel
[October 24, 2012 - October 24, 2012]
Medical and Pharmaceuticals
»
Clinical Products
TBA
Wilmington,
Delaware
[USA]
 Root Cause Analysis
GlobalCompliancePanel
[October 24, 2012 - October 24, 2012]
Medical and Pharmaceuticals
»
Analytical Products
TBA
Wilmington,
Delaware
[USA]
 Laboratory Water Systems Necessary Water Specifications and Validation Challenges
GlobalCompliancePanel
[October 23, 2012 - October 23, 2012]
Medical and Pharmaceuticals
»
Medical Devices
TBA
Wilmington,
Delaware
[USA]
 Reprocessing REUSABLE Medical Devices Cleaning and Labeling Requirements
GlobalCompliancePanel
[October 23, 2012 - October 23, 2012]
Medical and Pharmaceuticals
»
Medical Devices
TBA
Wilmington,
Delaware
[USA]
 EU Medical Device Classification
GlobalCompliancePanel
[October 18, 2012 - October 18, 2012]
Medical and Pharmaceuticals
»
Medical Devices
TBA
Wilmington,
Delaware
[USA]
 Residual Moisture Testing Proven Techniques
GlobalCompliancePanel
[October 18, 2012 - October 15, 2012]
Medical and Pharmaceuticals
»
Testing Products
TBA
Wilmington,
Delaware
[USA]
 SME Leaders Conclave Pune
Network 18
[October 17, 2012 - October 17, 2012]
Business Services
Hyatt Regency
Pune,
Maharashtra
[India]
 21 CFR Part 11 Ins and Outs of Audit Trails
GlobalCompliancePanel
[October 17, 2012 - October 17, 2012]
Medical and Pharmaceuticals
»
Pharmaceutical Products
TBA
Wilmington,
Delaware
[USA]
 Avoiding 483 Observations and Warning Letters
GlobalCompliancePanel
[October 17, 2012 - October 17, 2012]
Medical and Pharmaceuticals
»
Drugs
TBA
Wilmington,
Delaware
[USA]
 Medical Device Postmarketing Vigilance Reporting Update and Expectations for Manufacturers
GlobalCompliancePanel
[October 16, 2012 - October 16, 2012]
Medical and Pharmaceuticals
»
Medical Devices
TBA
Wilmington,
Delaware
[USA]
 Creating Material Waste and Personnel Flow Diagrams for Cleanrooms and Controlled Environments
GlobalCompliancePanel
[October 16, 2012 - October 16, 2012]
Medical and Pharmaceuticals
»
Medical Devices
TBA
Wilmington,
Delaware
[USA]
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Total 'Seminar' available now: 86 |
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