Webinar Recording: Panel Discussion: Exploring the retention guidelines within ICH E6 R3
Access the recording of 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 focussed 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
Instantly access the recording by filling out the form below:
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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