Medical device software process design

En kurs som erbjuds av en av våra nätverkspartners, QAdvis.

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The course is focused on how to design a process for development and maintenance of medical device software and maintaining it according to the requirements of the IEC 62304 standard and regulatory requirements for medical device software. 

Learning goals

  • To give hands-on understanding of current software practices and standards for compliance with regulatory demands
  • To give examples of efficient implementation of requirements to achieve compliance
  • To provide hints about future changes in the medical device software area


The focus of the course will be practical application of the requirements of the 62304 and ”how-to” make high quality software in a regulated enviroment.

Location

Stockholm: 26th and 27th March 2019
Location: Kista Entré Konferens, Knarrarnäsgatan 7, 164 40 Kista.
Time: Day 1 – 09:30– 16:30. Registration and coffee from 09.15.
Day 2 – 09:00-16:00.


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Besöksadress
Sveavägen 63, Stockholm

Postadress
Box 3601
103 59 Stockholm

Telefon 08-586 246 00 (vxl)

E-post info@swedishmedtech.se

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