thumb-webinar01

Tracking Medical Devices – How to Manage UDI Compliance Readiness

The first in a series of Webinars to discuss the important FDA regulatory compliance requirement for Tracking medical devices and UDI – Unique Medical Device Identifier requirements.

The Medical Device Tracking Symposium Series covers many topics throughout this coming year related to changing government regulations, industry guidance, infrastructure and technological challenges facing us all in this industry.

The Expert Panel Discussing the Following:

  • What is the FDA Final Rule on UDIs for medical devices and what does it mean for our industry?
  • What exactly is the Law (regulation) and what isn’t?
  • What are our timelines for compliance by device class and what are the expectations for compliance?
  • Anything under considerations that may affect this changing regulatory environment?
  • How can MedDevTrack help me with my compliance needs?
  • What is MedDevTrack plan to meet or exceed compliance requirements with their solutions?
  • Are there any publications available that I can take with me after the presentation to help further understand all of this in a deeper way?

View Slide Deck and Video Replay >

Register Today for the Complete Symposium Series

Please leave this field empty.

Membership Benefits:

  • Worldwide Regulation and Guidance Documents
  • Question and Answer Sessions from Device Industry Experts
  • Unlimited Access to the Complete Symposium Series Archive

YouTube Webinar

Slide Deck

Joe is the co-founder and CEO of A3 and brings over 30 years experience in Pharmaceuticals and Medical Devices with 25 years experience in medical Image systems development and automated image analysis. He has extensive experience with regulatory agency electronic submission systems and helped with the early specification of Optical NDA submissions and CANDA systems. Over the last five years, he has performed some ground-breaking work on Data Analytics & Visualization. He is available to provide expert consultation and management for the development and optimization of systems and business models supporting data collection, management and analysis and is a recognized expert in systems security. Joe brings experience in helping build solutions servicing almost the whole of pharmaceutical sectors, from Discovery through Manufacturing and Distribution, with particular expertise in Clinical Research and Post-Marketing Surveillance. He is adept helping bring sponsors into compliance; from his experience of learning it by living it. This is the fourth successful CRO venture that Joe has been involved with either as a founder or principal. Among a few of his areas of proven specialization over the years include: Data Analytics and Visualization, Medical and Document Imaging Systems, metadata-driven clinical database development, software development life cycle processes and documentation, cross-department pharma/device process re-engineering consulting.

Leave a Reply