2-day In-person Seminar

Software Risk Management


September 24th & 25th, 2018

Time: 9:00 AM to 6:00 PM

Philadelphia, PA

Venue: DoubleTree by Hilton Philadelphia Airport


Director : Markus Weber

**Please note the registration will be closed 2 days (48 Hours) prior to the date of the seminar.

  Price: $1,495.00
(Seminar Fee for One Delegate)

  Register for 5 attendees   Price: $4,485.00
      $7,475.00 You Save: $2,990.00 (40%)*

  Register for 10 attendees   Price: $8,222.00
      $14,950.00 You Save: $6,728.00 (45%)*
Course "Software Risk Management" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.

The seminar will address the specific challenges software poses for the risk management process. Basic risk management concepts will be introduced and then applied to software specific applications.


Why you should attend:

Risk Management is a regulatory and statutory requirement for medical devices. The generic procedure to perform risk management is outlined in ISO14791, however, as soon as software is used challenges arise. How to address these specific software issues and the application of FDA and IEC requirements for development of safety-critical software used in medical devices is the content of this seminar.


Who Will Benefit:

  • Project managers
  • Software Engineerrs
  • Regulatory specialists
  • Quality assurance specialists
  • Documentation specialists
  • Test managers
  • Software team leaders and lead developers


Day 1 Schedule


Lecture 1 (90 Mins):

Legal and regulatory requirements for risk management

Risk management and quality systems


Lecture 2 (90 Mins):

Risk Management Basics

  • What are hazards / hazardous situations
  • Hazard characteristics
  • Risk and risk rating
  • Residual risk

Lecture 3 (90 Mins):

Software failures

  • Random and systematic faults
  • Fault control means
  • Software failure effects

Lecture 4 (90 Mins):

System Architectures

Software Architecture

Software Tools and Methods

Multiprocessor systems

Real-time challenges


Day 2 Schedule


Lecture 1 (90 Mins):

Software Criticality Classification

  • IEC criticality classed
  • FDA level of concern

Lecture 2 (90 Mins):

The 62304 Development Process

  • Life Cycle
  • Documentation

Comparison to FDA requirements


Lecture 3 (90 Mins):

Software Risk Management

Software Configuration Management

Software Problem Resolution

Software Maintenance


Lecture 4 (90 Mins):

Legacy Software

Risk-based verification

Third-party software (SOUP, COTS)


Want to register by P.O/Check?
We facilitate registration by P.O/Checks!
Complete your registration in just a few easy steps
Please just download, fill out the registration form and send it to us either by email to support@globalcompliancepanel.com or just fax us at 302 288 6884.
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Following this just send us your purchase order by fax at 302 288 6884
Click here to download Registration form
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In case you wish to register by using check, please make a check to NetZealous LLC DBA GlobalCompliancePanel.com and mail it to the below address.
NetZealous LLC,
DBA GlobalCompliancePanel,
161 Mission Falls Lane,
Suite 216, Fremont, CA 94539, USA
Phone: 1800 447 9407

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Group participations
Get fabulous discounts by participating in groups of two or more.
No Attendees Discount
1 2 Attendees 10% off
2 3 to 6 Attendees 20% off
3 7 to 10 Attendees 25% off
4 10+ Attendees 30% off

To avail the above group discounts, all the participants should register by making a single payment

Call our representative TODAY on 1800 447 9407 to have your seats confirmed!

Markus Weber

Principal Consultant, System Safety Inc.

Markus Weber, Principal Consultant with System Safety, Inc., specializes in safety engineering and risk management for critical medical devices. He graduated from Ruhr University in Bochum, Germany with a MS in Electrical Engineering. Before founding System Safety, Inc., he was a software safety engineer for the German approval agency, TUV. Since 1991, Mr. Weber has been a leading consultant to the medical device industry on safety and regulatory compliance issues, specifically for active and software-controlled devices. In conjunction with the FDA, he has published works on risk management issues and software-related risk mitigations. Mr. Weber has helped multiple companies, from startups to Fortune 500 firms.

Location: Philadelphia, PA Hotel: DoubleTree by Hilton Philadelphia Airport   4509 Island Avenue, Philadelphia, PA 19153

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