Epista Life Science will participate at the DIA Regulatory Submissions, Information, and Document Management Forum (RSIDM) 2026, where regulatory leaders come together to discuss how submissions, data, and document management are evolving in response to rising regulatory expectations.
At RSIDM, we engage with peers across Regulatory Affairs, Regulatory Operations, and RIM to exchange experiences on topics such as structured submissions, regulatory data readiness, and modern document and information management. These discussions reflect the challenges many teams face today: increasing complexity, tighter timelines, and growing demands for consistency and transparency across markets.
Our team brings hands-on experience from inside regulatory organizations, combining regulatory expertise with deep knowledge of systems, data, and processes. We focus on what works in practice, helping regulatory teams strengthen their foundations, reduce manual effort, and prepare for what’s next without losing sight of daily operational realities.
If you are attending RSIDM 2026, we look forward to connecting and exchanging perspectives on how regulatory operations can become more efficient, resilient, and future-ready.
