BIVDA’s Regulatory Affairs Manager, Ashleigh Batchen, will be a keynote speaker at ‘The IVD School’, which will run from 28-30th March.
The training course, part of the MedTech Series, will navigate through the entire in vitro diagnostic lifecycle in 3 days of sessions: from introductions to all stakeholders in the in vitro diagnostic ecosystem, regulatory pathways for diagnostic approval and post-market considerations.
Additionally, benefit from engaging with eight specialised trainers, all of whom have extensive first-hand experiences with bringing in vitro diagnostic to market and adhering to the complex global regulatory landscape.
Ashleigh will be speaking on a number of topics, including: IVD classification and regulation, the impact of environmental legislation on the IVD industry, and working with trade associations as a ‘collective voice’.
Members can find out more information, including how to enroll, by visiting this page.