Date
21 October 2026Location
Online via Webex at 13:00 - 14:00About the event
This drop-in session explored the fundamentals of deviation investigation and how to establish root causes.
Why it’s important
This webinar helped attendees understand:
- the process of deviation investigation
- how to establish root causes
- how to write the deviation report
Intended audience
This session was aimed at:
- aseptic services and radiopharmacy services teams
- production and QA/QC teams
- authorised and accountable people
Speakers
The session included a presentation and a Q&As session supported by members of the SPS QA team.
Register
Registration is now closed.
Resources
The live Q&As are an opportunity during the webinar only. Our pre-recorded Quality Assurance presentations are available on our quality assurance for aseptic services videos page and our temperature management for medicines storage video page.
Contact us
Please contact the QA team if you have any questions.