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From GlobalCompliancePanel
Japan - Regulatory Filing Requirements and Compliance Processes for Life Sciences - Part I and Part II - Webinar By GlobalCompli
...Principles
o GCP
o GMP
o CTD / e-CTD Submissions
* Starting-Up and Conducting Clinical Trials
o Clinical Trial Start-Up process
+ Japan's Effort to Reduce "The Drug Lag"
+ Japan's Desire to Eliminate Bridging Studies and Participate in Ph. III Global Trials
Agenda for Part II:
Japan - Understanding the
more...
