Clinical trials continue to grow in cost, involvement, scope and complexity. Couple that with turnover and increased scrutiny from clinical trial inspections and one thing is certain: they need some continued maintenance. It’s now more important than ever to ensure the trials eClinical systems are on the right path, run smoothly and reach the right patients at the right time.
This webinar will take attendees through the what, why and how of putting together a care plan for a clinical trial. The featured speaker will discuss some great methodologies and some that are best left on the side of the road.
Matthew Lowrie, QA Manager, ASQ CQA, Almac
Matt has 20 years of experience within the pharmaceutical world with an extensive focus on regulatory inspections, auditing, software, and risk management.
Who Should Attend?
(All from Sponsor/Pharma/Biotech/CRO companies)
What You Will Learn
- What are regulators and inspectors actually looking for in a trial when it comes to the interactive response technology (IRT)?
- Stories from Almac’s experiences! (700+ clients, 3000 trials, 300+ inspections over the last three years)
- Why it’s not enough and not reasonable to just utilize audits as an oversight
- How to build a care plan for a trial: what works well for oversight, and what doesn’t work well
Almac Clinical Technologies
For over 20 years Almac Clinical Technologies group has been leading the Interactive Response Technology industry, bringing together the most innovative technology and our unparalleled expertise to empower biopharmaceutical industry and help bring new therapies to patients.