Online Training 2015 - Best Practices for FDA-Compliant Cybersecurity Management for Premarket Submissions of Medical Devices. - By Compliance Global Inc

Overview:
This webinar is intended to help you get familiar with the FDA-compliant management of medical device cybersecurity for regulatory purposes.
This webinar is further intended to increase our awareness that effective management of cybersecurity can greatly reduce the risk to patients by reducing the likelihood of compromising cybersecurity whether it is intentional or unintentional.
This webinar will address the best practices for cybersecurity management for premarket submission purposes concerning medical devices containing software as well as software that is a medical device.
The speaker will walk you through the FDA guidance practices.
Why Should You Attend:
To adequately manage cybersecurity for your medical devices containing software so that patient safety risks can be minimized.
Areas Covered in the Session:
? Laws and Regulations
? Definition
? Cybersecurity Principles and Functions
? Key Functional Requirements for Cybersecurity
? Regulatory Requirements
? Documentation
? Relevant and Applicable Standards
? Best Practices: Do’s and Don’ts
? PASS-IT Recommendations
Learning Objectives:
To understand and better manage cybersecurity for your medical devices containing software for premarket submission purposes.
Who Will Benefit:
? Regulatory Affairs Professionals
? Healthcare Professionals
? FDA Professionals
? Quality Professionals
? Medical Device Design Professionals
? Medical Device Scientists and Engineers
? R&D Professionals
? Complaint and Risk Management Personnel
? Consultants
? Contractors/Subcontractors
? CEOs
? VPs
? Clinical Affairs Consultants
? Other Interested Parties
Level:
Intermediate
For more detail please click on this below link:
https://www.complianceglobal.us/product/700078
Email: referrals-AT-complianceglobal.us
Toll Free: +1-844-746-4244
Tel: +1-516-900-5515