About this Event
Date: Dec 20,2024
Time: 1PM -2:30 PM ET
Duration: 90 Mins
Description
Is the new Quality Management System Regulation (QMSR) leaving you confused about compliance for your medical devices? You're not alone.
Don't let regulatory hurdles delay your product launch or limit your market reach! This exclusive webinar, led by a renowned FDA compliance expert, will equip you with the knowledge and tools to navigate the QMSR with confidence.
In this webinar, you will learn:
• The Impact of QMSR: Understand the key changes and how they affect your medical device manufacturing processes.
• Streamlined Compliance Strategies: Discover practical steps to implement the QMSR efficiently and minimize disruption.
• Cost Savings & Competitive Advantage: Learn how streamlined compliance can save you money, accelerate product launches, and give you a competitive edge.
• Global Market Access: Explore how aligning with ISO 13485 simplifies entry into international markets.
• Q&A with the Expert: Get your specific questions answered by our experienced speaker during the live session.
Bonus Materials:
• QMSR Implementation Checklist: Ensure a smooth transition with our downloadable checklist.
• Webinar Slides: Review the content at your convenience for future reference.
Who Should Attend:
• Medical device company CEOs, presidents, and executive teams
• Quality assurance and regulatory affairs professionals
• Engineers and product development teams involved in medical device manufacturing
Invest in Your Future:
This webinar can save you countless hours of research, frustration, and potential financial setbacks. Gain the knowledge and confidence to ensure smooth compliance and unlock global market opportunities for your medical device business.
Space is Limited - Register Today! -- Contact Us via Chat to Learn About the Early Bird Discount!
Event Venue
Online
USD 259.00 to USD 777.00
