Regulation of Electrical, Electronic and Software Devices

Regulation of Electrical, Electronic and Software Devices
Module 20 of the MSc and Masterclass: This Masterclass will enable you to understand the practical and strategic regulatory issues relating to the development, maintenance and marketing of active devices. It will enable you to critically debate the commercial implications and the impact of the regulations on product stakeholders.

: 29 Sep - 1 Oct 2021
Where: Online

Day 1 start time: 
13:00 GMT
Day 3 end time: 16:00 GMT

Also available as face-to-face course, please click here for the face-to-face registration option

Course overview

This Masterclass will cover the legislative requirements for electrical, electronic and software devices and apps as well as the current guidance available. The practical considerations of designing, developing or gaining approval for these devices will be discussed. In particular, the regulation and approval of software devices is particularly challenging with limited guidance available and very few experienced professionals, the challenges and hurdles will be explored as well as some potential solutions and areas in which more guidance is needed.

Benefits to delegates

This course will enable you to:

  • Demonstrate a systematic knowledge, and a critical awareness of the theory and practice of active device regulation
  • Be able to determine and justify which classification an active medical device falls into and identify the relevant conformity assessment procedure
  • Critically evaluate the regulations and their impact on development, maintenance and marketing of active devices
  • Understand the importance and content of key medical electrical equipment and systems safety standards and possess a comprehensive understanding of the unique issues relating to active devices and their use
  • Demonstrate the ability to critically analyse the legal documentation and regulatory considerations for active devices
  • Application of international and national standards for safety and performance requirements
  • Critically appraise and evaluate communications from regulatory bodies and research publications covering active devices
CPD: This course provides 19 CPD hours upon successful completion. To learn more about why Continuing Professional Development is important, visit our Lifelong Learning page.


The programme is available to download HERE

Module Leader


Suitable for

  • Students of the TOPRA MSc programme
  • Delegates from the regulatory affairs industry who wish to develop their knowledge of the regulation of electrical, electronic and software devices
  • Delegates from allied industries who wish to have a comprehensive understanding of the subject



    • TOPRA MSc students: £1,500+VAT*
    • Delegate: £1,700+VAT*

    Discounted places

    A limited number of discounted places are available at the rates below. Please email us at for a discount code before making your booking.

    • Those working for regulatory agencies, government agencies or academic institutions: £1275+VAT
    • Those working for charities, patient groups or in full-time education: £1275+VAT

    *VAT, if applicable, is charged at the rate of 20%.

    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.

    29/09/2021 - 01/10/2021
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