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UID:20261028T212253Z - 70497@odoo-54dc9f858c-c7xvh
DTSTART;TZID=Europe/Stockholm:20261125T090000
DTEND;TZID=Europe/Stockholm:20261126T160000
CREATED:20261028T212253Z
DESCRIPTION:<a href="https://package-1.intertek.test.cloudworkz.eu/event/me
 dical-device-software-process-design-based-on-iec-62304-130/register">Medi
 cal device software process design based on IEC 62304 </a>\nThis course fo
 cuses on how to design a process for the development and maintenance of me
 dical device software according to the IEC 62304 standard and the regulato
 ry requirements that apply to medical device software. TopicsCurrent softw
 are practicesDesigning high quality software in a regulated environmentSta
 ndards for regulatory complianceImplementation examples for achieving comp
 liancePractical applications of the requirements of the 62304 standardSome
  possible future changes within the medical device software field Target g
 roup This course is targeted towards professionals working with the develo
 pment of medical devices containing software or software as a medical devi
 ce (SaMD)\, with risk assessment of software-based products\, quality assu
 rance\, process improvements\, with the purchasing of software development
  from subcontractors\, or purchasing software components. Educational goal
 s After the course\, participants will have an understanding of how to emp
 loy design processes for medical device development based on the 62304 sta
 ndard\, in order to achieve regulatory compliance and how to design high q
 uality software in a regulated environment. Recommended prior knowledge A 
 basic understanding of the medical device regulations and some product and
  software development experience is recommended. ​ Course presentations 
 Course material will be in English\, verbal presentation in English. Cours
 e leaders The training is conducted in collaboration with Aurevia. Please 
 note: Intertek operates under strict standards of independence\, impartial
 ity\, and integrity. Read more about how we work here: https://www.interte
 k.com/about/co​mpliance-governance/ Upcoming courses See all Your Dynami
 c Snippet will be displayed here... This message is displayed because you 
 did not provide both a filter and a template to use.
DTSTAMP:20261028T212253Z
LOCATION:Intertek Semko AB\, Torshamnsgatan 43\, Kista  16440\, Sweden
SUMMARY:Medical device software process design based on IEC 62304 
X-ALT-DESC;FMTTYPE=text/html:<a href="https://package-1.intertek.test.cloud
 workz.eu/event/medical-device-software-process-design-based-on-iec-62304-1
 30/register">Medical device software process design based on IEC 62304 </a
 >\nThis course focuses on how to design a process for the development and 
 maintenance of medical device software according to the IEC 62304 standard
  and the regulatory requirements that apply to medical device software. To
 picsCurrent software practicesDesigning high quality software in a regulat
 ed environmentStandards for regulatory complianceImplementation examples f
 or achieving compliancePractical applications of the requirements of the 6
 2304 standardSome possible future changes within the medical device softwa
 re field Target group This course is targeted towards professionals workin
 g with the development of medical devices containing software or software 
 as a medical device (SaMD)\, with risk assessment of software-based produc
 ts\, quality assurance\, process improvements\, with the purchasing of sof
 tware development from subcontractors\, or purchasing software components.
  Educational goals After the course\, participants will have an understand
 ing of how to employ design processes for medical device development based
  on the 62304 standard\, in order to achieve regulatory compliance and how
  to design high quality software in a regulated environment. Recommended p
 rior knowledge A basic understanding of the medical device regulations and
  some product and software development experience is recommended. ​ Cour
 se presentations Course material will be in English\, verbal presentation 
 in English. Course leaders The training is conducted in collaboration with
  Aurevia. Please note: Intertek operates under strict standards of indepen
 dence\, impartiality\, and integrity. Read more about how we work here: ht
 tps://www.intertek.com/about/co​mpliance-governance/ Upcoming courses Se
 e all Your Dynamic Snippet will be displayed here... This message is displ
 ayed because you did not provide both a filter and a template to use.
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