URGENT PANDEMIC INFORMATION

In light of the pandemic situation events until September 2021 are cancelled. We will inform customers directly when the events are rescheduled.    
COVID CANCELLED: Project Management in Human Resources,   Boston MA, Jan 6-8, 2021
COVID CANCELLED: InterDrone, The International Drone Conference,   Cambridge MA, Jan 11-13, 2021
COVID CANCELLED: Supplier Management for Medical Device Manufacturers,   Cambridge MA, Feb 2-4, 2021
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Following events are tentatively planned but may be rescheduled, based on CDC guidelines or attendee registration interest .    
TENTATIVE: 21 CFR Part 11 Compliance,   Boston MA, Sep 22-24, 2021
TENTATIVE: Quality Control Laboratory Compliance,   Boston MA, Oct 6-8, 2021
TENTATIVE: Analytical Instrument Qualification and System Validation,   Boston MA, Nov 15-17, 2021
TENTATIVE: FDA's New Import Program for 2021,   Boston MA, Dec 7-9, 2021

Boston Professional Events List


What are Standards for Medical Device Software -2020


Date
Oct 12, 2021 - 10:00 AM
Organizer
Netzealous LLC DBA - Compliance4All
Venue
online
Location
Netzealous LLC DBA - Compliance4All,

Fremont,
CA,
US,
ZIP: 94539
Phone: 18004479407

Ticket Price: $ 150.00
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]

Full Details & Registration Link:

http://www.compliance4all.com/control/w_product/~product_id=501522LIVE?channel=eventztoday_Oct_2020_SEO

Event Categories
Keywords: HealthCare , medical, softwar




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