5th Annual ComplianceOnline Medical Device Summit 2020

Thursday, Apr 16, 2020 at 8:00 AM to Friday, Apr 17, 2020 at 5:00 PM EST

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Summit One Registration - Early Bird Partial Approval - $999.00

(For Registrations till January 15, 2020 - $999) (For Registrations after January 15, 2020 - $1499)

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Summit One Registration Partial Approval - $1,499.00

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Thursday, Apr 16, 2020 at 8:00 AM to Friday, Apr 17, 2020 at 5:00 PM EST

Innovate novel ideas for advancements in medical device technologies without compromising their safety and effectiveness. This summit brings together some of the renowned R&D experts and technology innovators to share information regarding opportunities, obstacles, best practices and challenges in the development of the new devices. Attendees will get insight into device innovation trends and upcoming changes in the medical device regulations.

 

Why you should attend this summit

  • Future Trends of Medical Device Regulation, Risk Management, UDI, Recall Complaint Management etc.
  • Listen from FDA/CDRH Directors:
    • What is Critical to Quality
    • Get Update on FDA compliance
  • Listen from FBI:
    • Cyber Security Risks
  • Learn More about Medical Device Global Regulatory Landscape and Off-label Promotion
  • Explore Upcoming Changes in Medical Devices under Trump Administration
  • Change Management
  • Criteria for Supplier Quality Agreement
  • Establishing a Medical Device Security Program
  • Panel Discussion
    • FDA Warning Letter
    • FDA Enforcement
    • FDA Interaction

For More Details:

https://www.complianceonline.com/medical-device-summit-seminar-training-80231SEM-prdsm?channel=eventzilla

At ComplianceOnline, we are focused on: Enhancing global compliance, creating a world where quality and compliance professionals, regulators, and government agencies come together to help the world comply with the intent and the spirit of laws, policies and mandates, ensuring continuous improvement in global operations, quality & safety. Making sure that we are responsible corporate citizens helping our constituents build a more responsible enterprise, one which operates with high quality , under a code of ethics, and with process discipline to ensure greater shareholder returns. Keeping things simple and straight forward , so that we all can indeed improve the quality of our processes, our work, our businesses and enhance compliance globally. Being inclusive, giving the process experts ( & novices! ), compliance professionals, quality champions, and regulatory agencies a voice so that all of us can contribute and make a difference.

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