FDAnews Announces — Sustained Medical Device Regulation Compliance: Ensure Your Regulatory Processes and Tools are Fully Optimized, Sponsored by Instem, Webinar, May 20
Summary
Implementation of EU-MDR and IVDR will exponentially increase the volume and velocity of data that requires regulatory operations support. Now is the time to challenge the status quo and leverage technology solutions to improve the efficiency of regulatory operations information management. Kim Young, Instem’s Director, Global Regulatory Intelligence, and Chris Nichols, an Instem Product Specialist, will explain the critical steps of confirming MDR readiness and remaining compliant with the new regulation. They’ll share how Regulatory Information Management (RIM) software can reduce several weeks of manual efforts into just a few hours — if not minutes. Pharmaceutical and medical device professionals rely on FDAnews print and electronic newsletters, books and conferences to stay in compliance with international standards and the FDAs complex and ever-changing regulations
Classifications
AskAI Classifications
LabelsLinked Companies
