- Do you have to get medical device regulatory approval for your app?
- What about your software – is it a medical device?
- Who is setting the standards and what precisely are they in the UK?
Join SEHTA for this digital health regulatory workshop and get your questions answered.
09:30 Registration and Refreshments
10:00 Welcome and Introduction by Chair, Dr David Parry, CEO, SEHTA
10:10 Information governance issues when working with health data, Chris Alderson, Partner, Hempsons
10:30 Overview by NICE on their Digital Health Technologies work, Harriet Unsworth, Senior Technical Analyst, NICE
10:50 mHealth apps – The landscape of regulation and review, Liz Ashall-Payne, CEO & Founder, ORCHA
11:00 Refreshment break
11:30 Digital Health Regulations – Evidence… the quest for the Holy Grail, Neelam Patel, COO, MedCity & Robert Turpin, Health Market Development Manager, BSI
11:50 SME Case Study – Docobo, Tom Muller, Customer Relations Executive, Docobo Ltd
12:30 Networking Lunch
SEHTA Member: £25 + VAT
Non Member: £50 + VAT
Please note that places are limited and only one person per company should apply for an invitation. You will receive confirmation of your place by Friday 20th October. An invoice will be sent to you once your place has been confirmed.
To apply to attend, please click here.