A leaftlet promoting the event "A guided walk through CEN/TS 17626:2021 for microbiome DNA analysis"
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A guided walk through CEN/TS 17626:2021 for microbiome DNA analysis

14 September @ 11:30 - 12:45 CEST
A leaftlet promoting the event "A guided walk through CEN/TS 17626:2021 for microbiome DNA analysis"

The webinar will take place on 14 September 2026, 11:30-12:45 CEST

ATTENTION:

  • Registration is open until the end of the business day on 9 September 2026.
  • To attend the live webinar, participants must possess a copy of CEN/TS 17626:2021 for licensing purposes.

Summary:

The webinar series is held in the context of the EU project CaBRIOH and co-organised by CaBRIOH project partner Medical University of Graz (BBMRI.at coordinator) and the BBMRI-ERIC Academy. It focuses on the European Technical Specification “Molecular in vitro diagnostic examinations – Specifications for pre-examination processes for human specimen – Isolated microbiome DNA”. It gives insight into the document clause by clause and provides as background information scientific evidence and rational as well as practical tips for users of CEN/TS 17626.

Part 1: Clause 1 “Scope”, Clause 4 “General considerations”

 

Speaker

Dr. Uwe Oelmueller

Host

Dr. Maike Tauchert

After watching the webinar, participants will have acquired the following knowledge:
  • Understand why a dedicated pre-analytical standard for microbiome DNA analysis is needed, and what it can and cannot deliver
  • How scientific evidence drives the development of standards
  • Navigate the structure, scope, and normative language of CEN/TS 17626:2021
  • General requirements for examination (analytical test) workflow developments, and how to use pre-examination workflow components (e.g. collection devices, nucleic acid isolation) for in vitro diagnostic (IVD) examination and for laboratories’ own developments
  • “Specification”, “verification” and “validation”- how they build the backbone for IVD product and laboratories’ own developments
  • Understand the role of risk management for IVD products and for laboratories’ own developments
  • Different responsibilities for IVD developers & manufacturers, and for medical laboratories developing own procedures

Register here!

Details

Date:
14 September
Time:
11:30 - 12:45
Event Categories:
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