FDAnews Announces — Digital Innovation: Revolutionizing Device Regulation Webinar, Oct. 5, 2016

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The increased connectivity of medical devices is transforming the regulatory landscape for device manufacturers. Join Tim Gee, Principal and Founder of Medical Connectivity Consulting, on Oct. 5 when he’ll provide insight into the regulatory landscape and recommendations for going forward.

Digital Innovation:
Revolutionizing Device Regulation
**An FDAnews Webinar**
Oct. 5, 2016 — 1:30 p.m. – 3:00 p.m. ET
http://info.fdanews.com/digital-innovation-pr

The increased connectivity of medical devices is transforming the regulatory landscape for device manufacturers. Mobile apps.. Remote monitoring… Wireless sensors… Messaging middleware.

What does this transformation mean for devicemakers?

Join Tim Gee, Principal and Founder of Medical Connectivity Consulting, on Oct. 5 when he’ll provide insight into the regulatory landscape and recommendations for going forward.
After attending this 90-minute webinar attendees will:

  •     Understand how remote monitoring, patient-generated data and mobile apps are the revolution in electronic medical records and how they are changing the everyday lives of regulatory affairs specialists
  •     Learn how miniaturization, wireless sensors and messaging middleware are changing the regulatory landscape and making speed to market more important than ever before
  •     Deal with the impact of the dramatic changes in OTS-IT software, HIPAA requirements, cybersecurity concerns, verification testing and post-market requirements into regulatory plans and programs
  •     Incorporate expert recommendations in the following key areas: product roadmaps; HIPAA audits; control gap analysis; verification testing; and regulatory strategy

Register today and optimize time-to-market and significantly reduce sustaining engineering costs.

Meet the Presenter:
Tim Gee is principal and founder of Medical Connectivity Consulting (MCC). Tim’s practice revolves around workflow automation through the integration of medical devices with information systems, and enabling technologies. MCC provides strategy development, business planning, business development, process optimization, technology selection and product management for vendors serving ambulatory and acute care providers. Needs assessment, solution specification, process reengineering and vendor selection represents MCC’s services for health care providers.

Who Will Benefit:

  •     RA personnel
  •     QA/QC personnel
  •     Data management and statistics personnel
  •     Engineering and design controls teams
  •     Risk management specialists
  •     Compliance officers

Webinar Details:
Digital Innovation:
Revolutionizing Device Regulation
Oct. 5, 2016 — 1:30 p.m. – 3:00 p.m. ET
http://info.fdanews.com/digital-innovation-pr

Tuition:
$287 per site

Easy Ways to Register:
Online:     http://info.fdanews.com/digital-innovation-pr                            
By phone: 888-838-5578 or 703-538-7600

About FDAnews:
FDAnews is the premier provider of domestic and international regulatory, legislative, and business news and information for executives in industries regulated by the US FDA and the European Medicines Agency. Pharmaceutical and medical device professionals rely on FDAnews' print and electronic newsletters, books and conferences to stay in compliance with international standards and the FDA's complex and ever-changing regulations.

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Michelle Butler
FDANEWS
+1 (703) 538-7665
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