GET THE ULTIMATE CLINICAL TRIAL TRACKING CHECKLIST
October 09, 2025 | 10 AM EST
Missed OpTImize London? We have you covered.
Join Daliah Botzkowski, Head of QA at iOnctura, along with Gill Gittens and Laurel-Ann Schrader, for a focused recap that turns event insights into practical next steps for your Trial Master File.
We will show how to plan and validate migrations with strong metadata mapping, document integrity checks, system compatibility reviews, and audit trail preservation so completeness and GCP compliance stay intact. We will clarify inspection readiness through strategic study reconstruction, including how to spot gaps, issue GCP corrections, log quality issues, and prepare for audits with confidence. You will also hear the view from CRO leaders on roles, collaboration, and sponsor oversight so teams reduce risk and keep the file ready. Leave with a compact playbook you can apply now to migrate with confidence, strengthen oversight, and align with partners across studies.
Gillian Gittens
Director, eClinical Strategy and Solutions
Laurel-Ann Schrader
Director, Client Solutions
Daliah Botzkowski
Head of QA at iOnctura