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| December - 2011 >> | ||||||
| Monday | Tuesday | Wednesday | Thursday | Friday | Saturday | Sunday |
| 1 Successful product complaint investigation (Global compliance panel) Ensure the safety of clinical trials (GlobalCompliancePanel) | 2 | 3 | 4 | |||
| 5 | 6 | 7 The controls for outsourcing manufacturing (Global compliance panel) Reprocessing reusable medical devices - cleaning (GlobalCompliancePanel) Leadership - in the non-leadership position (global compliance panel) | 8 Good documentation practice for GxP environments (GlobalCompliancePanel) Drug master files - understanding and meeting (GlobalCompliancePanel) Avoiding FDA 483 observations by identifying (global compliance panel) | 9 | 10 | 11 |
| 12 | 13 Design history file - DHF (GlobalCompliancePanel) | 14 | 15 New amendments of critical parameters (Global compliance panel) Troubleshooting ethylene oxide processes (GlobalCompliancePanel) | 16 | 17 | 18 |
| 19 | 20 Master production record requirements (GlobalCompliancePanel) | 21 How to prepare for, manage and follow-up to an FDI (GlobalCompliancePanel) | 22 | 23 | 24 | 25 |
| 26 | 27 | 28 | 29 | 30 | 31 | |
Successful product complaint investigation (Global compliance panel)
Ensure the safety of clinical trials (GlobalCompliancePanel)
The controls for outsourcing manufacturing (Global compliance panel)
Reprocessing reusable medical devices - cleaning (GlobalCompliancePanel)
Leadership - in the non-leadership position (global compliance panel)
Good documentation practice for GxP environments (GlobalCompliancePanel)
Drug master files - understanding and meeting (GlobalCompliancePanel)
Avoiding FDA 483 observations by identifying (global compliance panel)
Design history file - DHF (GlobalCompliancePanel)
New amendments of critical parameters (Global compliance panel)
Troubleshooting ethylene oxide processes (GlobalCompliancePanel)
Master production record requirements (GlobalCompliancePanel)
How to prepare for, manage and follow-up to an FDI (GlobalCompliancePanel)
Submit an event