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Reference Safety Information

Better understand basic aspects of the EU Regulation and Guidance that govern the content, placement, use, and management of the Reference Safety Information for assessing expectedness and causality to determine reportability of individual clinical trial cases.

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Registration fees

下方为企业参会人员价格。优惠价格适用于学术/非盈利机构和政府部门的工作人员。点击注册获知您的参会价格。请仔细阅读取消和转让注册条款。 Review the cancellation and transfer policy.

非会员价:
$350
会员价:
$300

Group Discounts

Group Rates and Licensing! DIA offers group rates to companies interested in purchasing eLearning modules for 10+ users! To request a proposal for multiple users, contact eLearning@DIAglobal.org.

On Demand Training Licenses

Individual registration is a license for individual access for 1 year from purchase.

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