Global regulatory demands for medical devices are increasing substantially, and regulatory teams are faced with the pressure of increased workloads and the need for more resources. To help regulatory professionals identify strategies and best practices in developing an effective and sustainable regulatory strategy for today’s global market, Medtech Intelligence is hosting the MedTech Regulatory Intelligence Summit on May 16-17 in Washington, DC.
Hear from RAQA professionals, regulators and industry leaders as they share strategies and best practices in developing a targeted regulatory model and finding solutions to key regulatory challenges throughout the product lifecycle—from streamlining the systematic review process to managing complaints, adverse event reporting and post-market study requirements.
The Summit will include examination of global regulations in the EU, China, Japan and UK, and how exporters can develop regulatory frameworks that incorporate the diverse range of requirements taking shape around the World.
Attendees can take advantage of networking opportunities, presentations from leaders in MedTech, and panel and small group discussions that will educate, inform and provide guidance on navigating current and forthcoming requirements.
Learn more and register here.
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