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Event has a status of Closed
CRED Understanding Digital Health and Electronic Products
Regulation on electrical, electronic and software medical devices.
When:
20 September 2018
Where:
TOPRA, 6th Floor, 3 Harbour Exchange, South Quay, London, E14 9GE, United Kingdom
What is it?
This course covers regulatory requirements for electrical, electronic, and software devices including current guidance, interpretation, and application of regulations. The practical considerations of design, development, and placement on market for these type of active devices will be discussed. In particular, the regulation and approval of software devices is particularly challenging with limited guidance available with continual advancement of technology.
Challenges and issues concerning active devices and software devices will be explored to discuss and review solutions that are being applied by regulatory professionals. The linkage between the electrical and electronic devices and software devices will also be described, with further presentation on how other processes like risk management, usability, and product life cycle management are linking everything together. Review of key requirements will be made including comparing and contrasting electrical, electronic, and software devices between US, European Union, and other countries.
Download a copy of the course programme here.
Who is it for?
This course is suitable for:
Any regulatory professional that works with active devices, specifically devices that are electrical powered, contain electronics, driven by software/firmware, or are software only applications.
Regulatory professional maintaining technical documentation or seeking approval for these types of devices.
What will I learn?
This course will provide an overview of electrical, electronic, and software devices examining different elements of regulatory requirements including:
Definition of “active” devices and components of electromechanical devices
Aspects implementing design controls applicable to active devices
Consideration of manufacturing activities for these type of devices
IEC 60601-1 standard and compliance needs
IEC 60601-1-2 standard and compliance needs
Safety and essential performance requirements
Marking and labelling of electromechanical and software devices
Usability and human factors to IEC 62366
Programmable Electronic Medical System (PEMS)
Linkage of electromechanical devices and software/firmware
Software Development Life Cycle to IEC 62304
Phases of software development, verification, and validation
IEC 62304 and FDA guidance document applicable to software
Software as a Medical Device (SaMD)
Software of Unknown Provenance (SOUP)
Risk management linkages for electromechanical devices and software
Networking and cybersecurity of software
Workshops and exercises to have regulatory professionals apply practical principles of electrical, electronic, and software devices
CPD:
8
How do I apply?
Simply
log in
or
create an account
and register below.
Course fees:
Type
Member
Non-member
Standard
£550+VAT
£675+VAT
Discounted places
A limited number of discounted places are available at the rates below.
Please email us at
meetings@topra.org
for a discount code
before
making your booking.
Those working for regulatory agencies, government agencies or academic institutions
£412.50+VAT
£506.25+VAT
Those working for charities, patient groups or are in full-time education
£275+VAT
£337.50+VAT
Terms and conditions
Please read the
training terms and conditions
before booking this course. By booking a place on this course you are agreeing to the
training terms and conditions
.
When
20/09/2018
Where
TOPRA 6th Floor, 3 Harbour Exchange South Quay London E14 9GE UNITED KINGDOM
Your company name
Your VAT country
Your VAT number
NOTE
Important instructions before booking -
If your company name or VAT number does not appear here or you would like to be invoiced using a different VAT number, please email
finance@topra.org
Register now
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