2012 APEC Advanced Workshop of Good Review Practice on Medical Products (Nov.6th-8th)

序號標題發布日期
1 Review Initiation Strategies in Your Agencies Part 22013-01-11
2 Review Initiation Strategies in Your Agencies Part 12013-01-11
3 How to Implement/Strengthen Pre-Filing Strategies2013-01-11
4 What Can PMDA do in early development stage of Medical Devices?2013-01-11
5 Review Initiation Strategy in TFDA/CDE2013-01-11
6 Post-Initial Review Strategies2013-01-11
7 Improving Regulatory Reviews EMA considerations2013-01-11
8 Review Initiation Strategies at Health Canada2013-01-11
9 The Review as a Continuation of the Development Process2013-01-11
10 Key Elements and Strategies2013-01-11
Total Records:10 Current Page No:1/ 1
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