Spotlight on IRT: Best Practices
by Matt Lowrie
August 31, 2020 11:00 pm
Mid-study protocol changes. Regulatory audit demands. Challenging technology integrations…Sound familiar? Today’s clinical trials are certainly more complex and demanding, and ensuring safety while saving time and money is something everyone wants. Too often in clinical development, we get caught up in our own processes and forget that there’s other ways to approach a problem. We know the struggles you have in the Interactive Response Technology (IRT) world and we want to help! Here at Almac Clinical Technologies, we are in a unique position to share some of the best practices we’ve seen from our wide and diverse client base. Join Matt Lowrie, your host for each episode of the Spotlight on IRT podcast, where he will answer your questions, discuss common pain points, and talk to industry leaders to help you drive efficiencies and prevent unnecessary risks.
Recent Episodes
Episode 14: Tips for Conducting an Effective Kick Off Meeting
4 years agoEpisode 13: Advantages of Agile Methodology
4 years agoEpisode 12: Checklist to ensure your IRT is inspection ready
4 years agoEpisode 11: Best Practices for Maintaining a Trial Master File
4 years agoEpisode 10: Umbrella Trial Designs: How to assess if your current IRT strategy can support them
5 years agoEpisode 9: Drug Pooling: How to Improve Cost Savings and Minimize Supply Outage
5 years agoEpisode 8: IRTechnophobia – [noun] Fear of full-service IRT providers
6 years agoEpisode 7: To Error is Human, But to Uncover The Root Cause is Divine; An In-Depth Look at IRT Software Investigations
6 years agoEpisode 6: Ensuring Right-Sized IRT Training for Any Sized Trial
6 years agoEpisode 5: Data Integrations: Everything you ever wanted to know but were afraid to ask
6 years ago