Panel Discussion: Exploring the retention guidelines within ICH E6 R3
Register for our Panel Discussion: Exploring the retention guidelines within ICH E6 R3.
The upcoming release of the finalised ICH E6 R3 guidelines on Good Clinical Practice (GCP) represents a major development for those involved in the management of clinical trials.
In this session our panel will focus on the significant changes and updates which will impact the retention of essential documents and data.
Our panel brings a broad range of experience and expertise from across the clinical trial landscape:
– Sara Thuresson – Head of Clinical Operations, Guard Therapeutics
– Suzanne Turner – TMF Consultant, Ice Consulting LLC
– Matthew Addis – CTO, Arkivum
Event Details:
– Date: Tuesday 22nd October 2024
– Time: 3pm BST 10am EST
– Register here:
As part of the registration process, you’ll have the opportunity to submit questions through the registration form. These questions may be included in the live discussion on Tuesday, 22nd October, giving you the chance to have your specific concerns addressed by our expert panel.
Anthony Wells
Anthony assumed the role of Product Marketing Manager at Arkivum in 2024, leveraging over a decade of experience of product marketing management in the technology sector. Proficient in developing and executing marketing strategies, Anthony is also experienced in product lifecycle management, from inception through to discontinuation.
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