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CQ5224 Global eCTD Management

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October 21, 2013, 3:45 am

CQ5224 Global eCTD Management

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CQ5224 Earlybird booking form

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October 22, 2013, 5:49 am

CQ5224 Earlybird booking form

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CQ5224TT52

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October 25, 2013, 7:20 am

CQ5224TT52

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CQ5224CO46

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October 25, 2013, 7:22 am

CQ5224CO46

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CQ5224TT46

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November 5, 2013, 5:44 am

CQ5224TT46

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CQ5224TT53

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November 5, 2013, 5:44 am

CQ5224TT53

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CQ5224TTJH

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November 5, 2013, 5:44 am

CQ5224TTJH

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Speaker Interview Series: 6 Things about you....

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November 28, 2013, 6:12 am

Speaker Interview Series: 6 Things about you....

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Speaker Interview Series Question 2

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December 5, 2013, 8:52 am

Speaker Interview Series Question 2

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6 things about Klaus Menges, Director, Federal Institute of Drugs and Medical...

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December 6, 2013, 7:18 am

6 things about Klaus Menges, Director, Federal Institute of Drugs and Medical Devices (BfArM), Germany

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6 things about Andreas Franken

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December 6, 2013, 7:18 am

6 things about Andreas Franken

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CQ5224KB15

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December 16, 2013, 2:10 am

CQ5224KB15

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'Current and future file formats for electronic submissions and archiving'...

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January 13, 2014, 7:21 am

'Current and future file formats for electronic submissions and archiving' Andreas Franken

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Speaker interview series: Question 3

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January 13, 2014, 8:07 am

Speaker interview series: Question 3

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Speaker interview series: Question 4

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January 13, 2014, 8:12 am

Speaker interview series: Question 4

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Fimea and e-Submissions Today and Tomorrow- Juha-Pekka Nenonen

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January 13, 2014, 8:17 am

Fimea and e-Submissions Today and Tomorrow- Juha-Pekka Nenonen

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A Case Study: Building best practice and steamlined MRP submissions- Shire...

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January 13, 2014, 8:18 am

A Case Study: Building best practice and steamlined MRP submissions- Shire Pharmaceuticals- Charmaine Reid

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Successful Planning for eCTD Lifecycle Management- Geoff Williams

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January 14, 2014, 1:59 am

Successful Planning for eCTD Lifecycle Management- Geoff Williams

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DHMA requirements and expectations - Mickel Hedemand, Danish Health and...

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January 15, 2014, 8:23 am

DHMA requirements and expectations - Mickel Hedemand, Danish Health and Medicines Authority

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Challenges ans experience with the new validation criteria - Mickel Hedemand,...

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January 15, 2014, 8:26 am

Challenges ans experience with the new validation criteria - Mickel Hedemand, Danish Helath and Medicines Authority

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