11.00 – 11.25 uur

(Engelstalige lezing) This presentation will present how Software as a Medical Device is defined in FDA and IMDRF guidances; benchmarked to the EU MDR & IVDR. Introduction to BSI’s SaMD team and the pathways and application timelines. Further definition of SaMD will be defined; and key GSPRs will be defined and shared from a notified body’s perspective.

  • Another section of the key standards will be explained and the combined processes. What wants the notified body to know in this part?
  • Moving on to key guidance, in the MDR; as well the significant changes explained
  • A section about technical file presentation; most common reasons for delays in technical documentation reviews

Spreker: Sreenath Sukumaran | BSI Group

FHI, federatie van technologiebranches
en_GBEnglish (UK)