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Medical Device Cybersecurity Regulatory Publications

Medical Device Cybersecurity Regulatory Publications

Colin Morgan       January 22, 2021      0 Comments

REGULATORY PUBLICATIONS LIST

Over the past few years, a number of Regulatory Authorities across the globe have published materials related to Medical Device Cybersecurity. We’ve been able to track down links to most of the publications we are aware of and are working on obtaining the ones that are missing. If there are any gaps in the list below, please email info@apraciti.com and we’ll make the necessary updates.

This information should enable Product Security teams to more easily find and review regulatory expectations related to Medical Device Cybersecurity.

(Please note, many of the links below take you to a government agencies website. They are not located within the apraciti.com domain)


CountryRegulatory AuthorityDocument TitleRelease DateLink
AustraliaTherapeutic Goods AdministrationMedical device cyber security guidance for industry2019
(July)
https://www.tga.gov.au/
publication/medical-device
-cyber-security-guidance-industry
BrazilGeneral Management of Health Products Technology (GGTPS)Guide 38/2020, Principles and Practices of Cyber Security in Medical Devices2020
(September)
https://www.gov.br/
CanadaHealth CanadaPre‐market Requirements for Medical Device Cybersecurity2019
(June)

https://www.canada.ca

ChinaNational Medical Products Administration (NMPA)Medical Device Network Security Registration on Technical Review Guidance Principle2017
(January)
 
ChinaNational Medical Products Administration (NMPA)Draft Technical guideline on medical device cybersecurity, Version II2020
(September)
 
FranceAgency for the Safety of Health ProductsCybersecurity of Medical Devices integrating software during their lifecycle2019
(July)
https://www.ansm.sante.fr/S-informe
r/Points-d-information-Points-d-inform
ation/L-ANSM-lance-une-consultat
ion-publique-sur-un-projet-de-reco
mmandations-pour-la-cybersecu
rite-des-dispositifs-medicaux-Poi
t-d-information
GermanyGerman Institute for Drugs and Medical Devices (BfArM)Cyber Security Requirements for Network-Connected Medical Devices2018
(November)
https://www.allianz-fuer-cyb
rsicherheit.de/ACS/DE/_/d
ownloads/BSI-CS/BSI-CS_13
2E.html?nn=6656412
JapanPharmaceutical and Medical Device AgencyEnsuring Cybersecurity of Medical Device: PFSB/ELD/OMDE Notification No. 0428-12015
(April)
Japanese Version –
 https://www.pmda.go.jp
/files/000204891.pdf
JapanPharmaceutical and Medical Device AgencyGuidance on Ensuring Cybersecurity of Medical Device: PSEHB/MDED-PSD Notification No. 0724-12018
(July)
Japanese Version –
 https://www.pmda.go.jp
/files/000225277.pdf
JapanPharmaceutical and Medical Device AgencyRecent Trends in Cybersecurity Assurance of Medical Devices No. 3732020
(June)
https://www.pmda.go.jp/fil
es/000235348.pdf#page=4
SaudiSaudi Food and Drug AuthorityGuidance to Pre-Market Cybersecurity of Medical Devices2019
(April)
https://www.sfda.gov.sa/a
r/medicaldevices/regulations/
DocLib/MDS-G38.pdf
SingaporeHealth Sciences AuthorityInformation Technology Standards Council Technical Reference 67: Medical device cybersecurity2018https://itsc.imda.gov.sg/
standards/singapore-it-
standards/
South KoreaSouth Korean Ministry of Science and ICTCyber Security Guide for Smart Medical Service (Link no longer working)2018
(May)
https://www.msit.go.kr/web
/msipContents/contentsView.do?cateId=mssw311&artId=1383336
TaiwanMinistry of Health and WelfareGuidance on Management of Cybersecurity in Medical Devices for Manufacturers2019
(November)
Chinese Version – https
://www.fda.gov
.tw/tc/includes/GetFile.ashx?id=f637099316577783149
United StatesUS Food and Drug AdministrationDraft Guidance: Content of Premarket Submissions for Management of Cybersecurity in Medical Devices2018
(October)
https://www.fda.gov/regu
latory-information/search
-fda-guidance-documents
/content-premarket-su
bmissions-manageme
nt-cybersecurity-medic
al-devices
United StatesUS Food and Drug AdministrationFinal Guidance: Postmarket Management of Cybersecurity in Medical Devices2016
(December)
https://www.fda.gov/re
gulatory-information/sea
rch-fda-guidance-docume
nts/postmarket-manage
ment-cybersecurity-
medical-devices
United StatesUS Food and Drug AdministrationFinal Guidance: Content of Premarket Submissions for Management of Cybersecurity in Medical Devices2014
(October)
https://www.fda.gov
/regulatory-informati
on/search-fda-guidance-document
s/content-premarket
-submissions-manage
ment-cybersecurity-medical-devices-0
United StatesUS Food and Drug AdministrationCybersecurity for Networked Medical Devices Containing Off-the-Shelf (OTS) Software2005
(January)
https://www.fda.gov
/regulatory-information/se
arch-fda-guidance-documents/cyberse
curity-networked-medical-
devices-containing-shelf-ots-software
OtherInternational Medical Device Regulators ForumIMDRF Principles and Practices for Medical Device Cybersecurity2020
(April)
http://www.imdrf.or
g/docs/imdrf/final/tech
nical/imdrf-tech-2003
18-pp-mdc-n60.pdf
EUMedical Device Coordination GroupMDCG 2019-16 Guidande on Cybersecurity for medical devices2019
(December)
https://ec.europa.eu/d
ocsroom/documents/38924
United StatesThe Office of the National Coordinator for Health Information Technology (ONC)Draft Medical Device Manufacturer Internet of Things (IoT) Code of Conduct2020
(January)
https://www.heal
thit.gov/topic/international-health-it-collaborations/draft-medical-device-manufacturer-internet-things-iot-code-conduct
 
 
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