A forum created and managed by the Drug Information Association (DIA) Electronic Regulatory Submissions (ERS) community that provides best practices guidance on electronic submission issues and supports development of tools that will aid stakeholders in complying with and understanding the guidance, specifications, and regulations associated with regulatory submission issues. Specifically, the blog will focus on Regional requirements, eCTD 4.0/RPS, CDISC/ADAM/SEND, iCSRs/IDMP
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