Navigating the new clinical trial regulations: ACCORD Q&A webinar

Details

This webinar offers researchers the opportunity to ask questions about ACCORD's updated Sponsor SOPs in preparation for the new UK Clinical Trial Regulations and ICH‑GCP E6(R3).

Over the coming months, updated SOPs will be released weekly, and this session will give you the chance to ask questions directly to the teams involved in developing and implementing these changes.

Representatives from Pharmacovigilance, Monitoring, Governance, and QA will be present to help clarify expectations and provide practical guidance.

To help us tailor the session, we encourage you to submit questions in advance - your input will shape the discussion and ensure we address the topics most important to you. You can submit questions via the registration form or by emailing them to  education@edinburghCRF.ed.ac.uk.

We look forward to seeing you there and supporting you through this period of transition.

Please note, this session will be recorded for administration purposes - however the recording will not be made available publicly. Instead, a document will be produced and shared following the event to capture pertinent questions and answers.