2019 - EN/IEC 62304 - Is your Medical Device Software Out of Compliance

Overview:
This course will ensure that you know what is expected to have in place for
compliance for your company during the preparation of a 510K to prevent
potential audit risks and serious findings post submittal that can block your
ability to sell your product successfully.
Why should you Attend:
This course will ensure that you know what is expected to have in place for
compliance for your company during the preparation of a 510K to prevent this
risk.
Who Will Benefit:
Director of Regulatory
Vice President of Quality
Vice President of Compliance and Regulatory
Regulatory Expert
Speaker Profile:
Nancy Knettell , Founder and Principal at SoftwareCyber510, LLC, has over 30
years in Software Development and Regulatory experience primarily in the IVD
and Medical Device industry for such major IVD and medical device companies
such as Genomic Health, BioRAD, Smith and Nephew, Philips Medical, CR Bard,
Kollsman Medical, and Johnson and Johnson.
Event Fee: One Dial-in One Attendee Price: US $150.00
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: compliance4all14-AT-gmail.com