health apps quality & reliability qadvis ab new technical ...€¦ · • investigation,...
TRANSCRIPT
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Health Apps Quality & Reliability
– new Technical Specification
EN ISO/IEC TS 82304-2© QAdvis
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Practical issues
• Presentation will be recorded
• Questions answered after the
presentation
• Short evaluation in the end
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Zoom webinar
Ask your
questions, via
‘Q&A’.
‘Chat’- used to get in
touch with the
administrator, will not be
answered by the
presenter.
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Agenda
• Presentation (30 min)
– Intro
– Background & Purpose
– Scope
– Content
– Status & timeline
• Q&A (15 min) © QAdvis
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QAdvis – Key competence areas
QMS In-the-cloud
Turnkey QMS
Digital Signatures
Efficient and Lean
System Development
Product Software Validation
Computer Systems Validation
Risk Management
Verification and Validation
Process Validation
QA&RA/Clinical Consulting
Interim Management, Expert Advise
Audits/Mock audit/Due Diligence
Warning Letters, Compliance Projects
PMA, 510k, CE-Marking, Tech Files
Global Regulatory Support
Vigilance, Recalls, PMS
Clinical Evaluation and Clinical Studies
Training/Courses
CE-Marking, MDR, IVDR
ISO 13485 & QSR & MDSAP
IEC 62304 & IEC 82304-1
IEC 60601-1
IEC 62366-1
Risk Management (ISO 14971)
And more…
Agile, Lean and Six
Sigma
Training and consulting
in cooperation with US
partner
European Authorised
Representation
Providing European representation
for non-EU MedTech companies
Active member of EAAR
(European Association of Authorized Reps)
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Presentation of the speaker Maria Rickardsson
• >20 years experience in regulatory frameworks, quality assurance and risk management in medical device, software and telecom
• Extensive experience from ISO 13485, ISO 14971 and IEC 62304
• Member of standardization committees for medical device software and medical device IT networks
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Why health apps need a new Technical
Specification
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Patient perspective
• Unclear what is the right App
get-ehealth.eu
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EU Single Market Strategy
https://ec.europa.eu/growth/single-market/european-standards/ict-standardisation
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National App Quality Frameworks
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Starting point - EN ISO/IEC TS 82304-2
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health
• state of complete
physical, mental and
social well-being and not
merely the absence of
disease or infirmity
Definition of HEALTH
www.who.int/about/who-we-are/constitution
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health software
• Software intended to be
used specifically for
managing, maintaining or
improving health of
individual persons,
or the delivery of care
Definition of HEALTH SOFTWARE
IEC 82304-1:2016
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Definition of App
App
• software application that can be
executed (run) on a computing
platform, and is typically a small
application run or accessed on
mobile devices
BSI PAS 277:2015, 3.1.1
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Scope of EN ISO/IEC TS 82304-2
Health
Apps
Health SW
Medical Device SW
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Definition of MEDICAL DEVICE
Any instrument, apparatus, appliance, software, implant, reagent, material or other article intended by the
manufacturer to be used, alone or in combination, for human beings for one or more of the following specific
medical purposes:
• diagnosis, prevention, monitoring, prediction, prognosis, treatment or alleviation of disease,
• diagnosis, monitoring, treatment, alleviation of, or compensation for, an injury or disability,
• investigation, replacement or modification of the anatomy or of a physiological or pathological process
or state,
• providing information by means of in vitro examination of specimens derived from the human body,
including organ, blood and tissue donations,
and which does not achieve its principal intended action by pharmacological, immunological or metabolic means, in or
on the human body, but which may be assisted in its function by such means.
The following products shall also be deemed to be medical devices:
• devices for the control or support of conception;
• products specifically intended for the cleaning, disinfection or sterilisation of devices as referred to in Article 1(4)
and of those referred to in the first paragraph of this point.
REGULATION (EU) 2017/745 on medical devices
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Scope of EN ISO/IEC TS 82304-2
Health
Apps
SW only
productsSW part of
HW products
Health SW
Medical Device SW
Apps for
other
Health use
Medical Device Apps
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Content – Quality Criteria
Quality Assessment Questions
Health App Quality Report
Quality Scores
Quality Label
Assessment
App Checkers
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Quality Assessment Questions
• Product informationA
• Clinical benefit and safetyB
• Accessibility and usabilityC
• Privacy and securityD
• Technical performance and interoperabilityE
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Score & Label
App identification
Benefit
Score
Contact
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Referenced standards
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Referenced standards
• IEC 82304-1Health software — Part 1: General requirements for product safety
• IEC 62304Medical device software — Software life cycle processes —Amendment 1
• ISO/IEC 27001Information technology — Security techniques — Information security management systems
• cMHAFFHL7 Consumer Mobile Health Application Functional Framework
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Standards relations
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IEC 82304-1 Health software —
Part 1: General requirements for product safety
• Requirements specification
• Software life cycle processes
• Validation
• Identification
• Accompanying documents
• Post-market activities© QAdvis
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Timeline
• August 2020 – DTS voting starts
• October 2020 – voting closed
• December 2020 – TS published
• Next edition?
DTS – Draft Technical Specification TS – Technical Specification
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Summary
• New Technical Specification by
end of this year
• Common Quality Assessment
Framework
• Help users
• Help App Developers © QAdvis
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QAdvis services
• Courses
– Medica Device SW process design (IEC 62304)
– CE - marking
– Technical Documentation
– IVDR / MDR
– Risk management,
– ISO 13485:2016
• Product specific workshop
• Internal trainings
• GAP analysis and implementation plan
• Quality Management System
• Auditing
• Risk management
• Clinical evaluation
www.qadvis.com/courses-and-seminars/
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Thank you for your attention!
Questions & Answers
Ask your
questions now, via
‘Q&A’.
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Evaluation
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