Sponsored webcast: Navigating the Complex IVDR Landscape (On-demand)

1.0 RAC Credits Member: $0 | NonMember: $25
Sponsored webcast: Navigating the Complex IVDR Landscape (On-demand)

With the IVDR coming into force on 26 May 2022, there are still many questions and challenges for IVD manufacturers facing the difficult task of implementing the new regulation. Our experts are here to help answer your most urgent questions.

This webinar will look closely at the requirements of the EU IVDR, timelines and deadlines and common pitfalls of technical documentation.

Learning Objectives

Upon the conclusion of the program you will be able to:

  • Understand the EU IVDR Requirements
  • IVDR timelines and deadlines
  • Technical Documentation common pitfalls

Who Should Attend?

  • Manufacturers
  • IVD companies

Audience Learning Level:

Intermediate: Content is designed based upon the assumption that individuals have basic knowledge of the topic(s) and/or demonstrated competence related to the topic(s). Higher-level concepts are introduced during lectures; exercises requiring synthesis and/or application of concepts are incorporated into the activity.


Elizabeth Harrison

Elizabeth Harrison,PhD, BSc
Global Head of IVD
BSI Group

Dr. Elizabeth Harrison is the IVD Global Head at BSI. Dr. Harrison is responsible for operational delivery of technical aspects of IVDD, IVDR and UKCA conformity assessments. She leads a global team of regulatory product experts, final reviewers and decision makers across all types of IVD medical device.

Prior to BSI, Dr. Harrison worked as a molecular biologist and product expert with specialism in infectious disease, human genetic testing, cancer and companion diagnostics.


For account support, contact the RAPS Support Center: +1 301 770 2920, ext. 200 (8:30 am–5:30 pm EST, Monday–Friday) or email support@raps.org.

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