2018 Medical Device Software Risk Management Seminar
In-Person Event
Sep 24 - 25, 2018
Philadelphia, Pennsylvania, USASpeakers
OVERVIEW
2018 Medical Device Software Risk Management Seminar is organized by GlobalCompliancePanel and will be held from Sep 24 - 25, 2018 at DoubleTree by Hilton Hotel Philadelphia Airport, Philadelphia, Pennsylvania, United States of America. This CME Conference has been approved for a maximum of 12 credits.
Overview:
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 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 the 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 Engineers
• Regulatory specialists
• Quality assurance specialists
• Documentation specialists
• Test managers
• Software team leaders and lead developers
Speaker:
Markus Weber
Principal Consultant, System Safety Inc.
Time: 9:00 AM to 6:00 PM
Price:
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%)
Overview:
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 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 the 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 Engineers
• Regulatory specialists
• Quality assurance specialists
• Documentation specialists
• Test managers
• Software team leaders and lead developers
Speaker:
Markus Weber
Principal Consultant, System Safety Inc.
Time: 9:00 AM to 6:00 PM
Price:
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%)
KEY DATES
24 Sep, 2018
Event Start Date
25 Sep, 2018
Event End Date
SPECIALITIES
Medical EducationRisk Management and Medical NegligenceQuality ManagementSUGGESTED HOTELS
CONFERENCE VENUE
DoubleTree by Hilton Hotel Philadelphia AirportRELATED CONFERENCES & LIVE WEBINARS
Quick Links