Sponsored Webcast: Regulations Change. Is Your QMS Ready?

Regulations change, customer expectations evolve, and businesses grow. Is your quality management system built to keep up? This webcast will explain how a global medical device contract manufacturer modernized its quality system to support multiple sites, diverse customer requirements in an increasingly complex regulatory landscape. Participants will get a reality check on today's quality challenges and what organizations should look for in an eQMS to support compliance, scalability, and long-term regulatory readiness.

2pm – 3pm EST 19 November 2026 + Add to calendar

Regulations change but is your QMS ready? Join this webcast to learn how Resonetics, a medical device manufacturer, built a quality system designed to adapt to changing regulations.

Customer expectations are evolving and businesses are growing. Is your quality management system built to keep up? Join Dan Miller, Quality Systems Analyst at Resonetics, as he shares how the global medical device contract manufacturer modernized its quality system to support multiple sites, diverse customer requirements, and an increasingly complex regulatory landscape. Jennifer Bianchini, Senior Product Marketing Manager at Octave (formerly ETQ), will deliver a reality check on today's quality challenges and what organizations should look for in an eQMS to support compliance, scalability and long-term regulatory readiness.

Learning Objectives

Upon completion of the webcast, participants will be able to::

Leverage ISO 13485 principles to build a scalable quality framework
Prepare for evolving regulatory requirements, including the transition to QMSR
Establish a foundation for validation, audit readiness and continuous improvement
Develop a quality system capable of supporting growth while maintaining compliance
Future-proof quality processes to adapt to changing business and regulatory demands

Who Should Attend?

This intermediate-level webcast is ideal for professionals in Regulatory Affairs, Quality Assurance, Quality Systems, Compliance, and Operations within the medical device and combination product industries.

Job titles may include: Regulatory Affairs Manager, Regulatory Affairs Specialist, Quality Manager, Quality Engineer, Compliance Manager, Quality Systems Administrator, and Operations Leader.

This webcast is particularly valuable for organizations seeking to modernize their quality management systems, strengthen regulatory readiness, support business growth, and adapt to evolving global quality and compliance requirements.

Audience Learning Level

Intermediate: Content is designed based upon the assumption that individuals have basic knowledge of the topic(s) and/or demonstrated competence related to the topic(s). Higher-level concepts are introduced during lectures; exercises requiring synthesis and/or application of concepts are incorporated into the activity.