GET THE ULTIMATE CLINICAL TRIAL TRACKING CHECKLIST
eISF 101: Digitizing Investigator Site Files for Better Compliance, Security, Efficiency
Learn what happens when ISFs go wrong and how digitizing them can save time and improve your audit readiness. You’ll laugh. You’ll cringe. You’ll never want to go back to paper.
Key Takeaways from OpTImize London
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.
Alleviating CRA Burdens with eClinical Innovation
Clinical research associates (CRAs) play a crucial role in the safety and ethics of drug development. However, administrative tasks and repetitive data entry often take time away from the impactful work they do.
Create, review, and archive clinical content. Launch compliance focused training. Index all required records in the eTMF
All within one system
Make it easy to show the story of your study to regulatory agencies.
