What are Standards for Medical Device Software - 2017

7 years ago Posted By : User Ref No: WURUR14094 0
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  • TypeWebinar
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  • Location Fremont, California, United States
  • Price
  • Date 10-10-2017
What are Standards for Medical Device Software - 2017, Fremont, California, United States
Webinar Title
What are Standards for Medical Device Software - 2017
Event Type
Webinar
Webinar Date
10-10-2017
Location
Fremont, California, United States
Organization Name / Organize By
Netzealous LLC DBA - Compliance4All
Organizing/Related Departments
Healthcare Training
Organization Type
Organization/Company
WebinarCategory
Both (Technical & Non Technical)
WebinarLevel
All (State/Province/Region, National & International)
Related Industries

Education/Teaching/Training/Development

Information Technology

Accounting/Financial/Banking/Insurance

Manufacturing

Location
Fremont, California, United States

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

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.

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: [email protected]

Others Details

For more details and updates please visit website.

Registration Fees
Available
Registration Fees Details
One Dial-in One Attendee Price: US$150.00
Registration Ways
Email
Phone
Website
Address/Venue
  Online 
Official Email ID
Contact
Event Manager

Online

[email protected]

     18004479407
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