In this free webinar, learn how an effective quality management system can support post-market surveillance, complaint handling and regulatory reporting after a medical device reaches the market. The featured speaker will discuss how to monitor device performance, identify safety signals and determine when an event requires Medical Device Reporting. Attendees will also explore how to respond to FDA inspections, Form 483 observations and Warning Letters while addressing underlying quality system deficiencies.
TORONTO, Aug. 24, 2026 /PRNewswire/ — Launching a medical device is only the beginning of its regulatory lifecycle. Once the device reaches users, manufacturers must maintain effective post-market surveillance, evaluate complaints and identify reportable events while keeping the quality management system current and inspection-ready. This webinar explores how an effective QMS supports these responsibilities after launch.
Attendees will examine the elements of a healthy post-market system, including processes for monitoring device performance, managing complaints and determining when an event requires Medical Device Reporting. The session will also address how quality and regulatory teams can maintain documentation, identify emerging signals and respond before isolated issues develop into broader compliance risks.
The webinar will also cover practical considerations following an FDA inspection, Form 483 or Warning Letter. Attendees will learn how to assess observations, prepare timely responses and address the underlying system weaknesses that contributed to the findings.
Register for this webinar to learn how a QMS can support post-market compliance, timely reporting and continued medical device availability.
Join Etienne Nichols, Head of Industry Insights & Education, Greenlight Guru, for the live webinar on Thursday, September 10, 2026, at 11am EDT (5pm CEST / EU-Central).
For more information, or to register for this event, visit Strengthen QMS Controls to Reduce Post-Market Compliance Risk.
ABOUT XTALKS
Xtalks – The Life Science Community™ empowers professionals across pharma, biotech, medtech, healthcare and research with the trusted knowledge and collaborative insights that move the industry forward. Powered by Honeycomb Worldwide Inc., Xtalks delivers news, feature articles, webinars, podcasts, videos, expert interviews, curated job opportunities and more designed to support informed decision-making in a fast-evolving sector.
Every year, thousands of professionals rely on Xtalks for timely intelligence, peer perspectives and industry thought leadership. Join our life science community to stay informed, connected and ready for what’s next.
To learn more about Xtalks, visit www.xtalks.com
For information about working with Xtalks to host your webinar, visit https://xtalks.com/partner-with-us/
Contact: Soumya Shashikumar
Tel: +1 (416) 977-6555 x371
Email: skumar@xtalks.com
View original content to download multimedia:https://www.prnewswire.com/news-releases/strengthen-qms-controls-to-reduce-post-market-compliance-risk-upcoming-webinar-hosted-by-xtalks-302857461.html
SOURCE Xtalks
