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What are Standards for Medical Device Software -2017

 
  August 09, 2017  
     
 
Netzealous LLC DBA - Compliance4All, Online
2017-10-10


Overview:  
With various changes to standards and regulations, it is important to 

understand the criteria for compliance, this is your DIY guide to the changes 

in standards, specifically covering the IEC 62304 standard.

Why should you Attend:
Why do all these documents exist, and how do they affect the work your 

group is doing on your company's software? What does a software group 

need to know about them, and what changes can we expect in the near 

future? 

Areas Covered in the Session:
Electrical equipment safety inevitably involves software
Usability requires us to understand who were working to help
Planned changes will adapt these standards to new challenges
Good engineering is our goal- compliance follows

Who Will Benefit:
Software Developers
Business Analysts
Requirements Analysts
Product Managers



Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com
 
 
Organized by: Event Manager
Invited Speakers:
Speaker Profile:
Brian Shoemaker consults for healthcare products companies on computer 

system validation, software quality assurance, and electronic records and 

signatures. He has conducted validation both on product software and on 

internal software, developed software quality systems, audited software 

quality processes (including agile methodology), and evaluated 21 CFR Part 11 

compliance.
 
Deadline for Abstracts: 2017-10-09
 
Registration:
Full Details & Registration Link:
 
E-mail: support@compliance4All.com
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