Patient Engagement Suite

41. Using IRT Data To Automate And Optimize Clinical Supply 4/17/2023

    Learn how clinical teams can save between $150,000 and $1 million in annual drug and shipping costs through automated supply optimization.

42. Providing Drug Supply Support In Complex Environments Through IRT 4/5/2023

    Learn how applying predictive data analytics can enable the creation of an ideal supply strategy capable of reducing the need for extra shipments, manual oversight, and supply waste.

43. How eConsent Improves The Trial Experience For Patients And Sites 4/5/2023

    In part one of this series, the author dives into how electronic consent platforms are simplifying and improving the trial experience for patients and sites.

44. Biosample Tracking: A Consenting Dilemma 3/7/2023

    Biosample collection is an inevitable part of most clinical trials. Learn how sponsors should be tracking every sample back to the source so as to not violate compliance issues.

45. 7 Considerations For eCOA Technology Solutions 3/3/2023

    Choosing the right vendor, solution, and deployment model is critical for a clinical trial to be successful. As a sponsor, consider these seven best practices when selecting the best eCOA.

46. eConsent For Complex Clinical Trials 10/31/2022

    Master protocol design trials require an endless stream of consent forms, adding time, cost, and risk. Learn how a feature-rich eConsent platform can simplify those processes and improve engagement.

47. eCOA Implementation Guidance For A Patient-Centric Experience 9/21/2022

    Historically, the patient perspective was captured during site visits, paper diaries, and questionnaires. Review today's platforms for collecting electronic clinical outcome assessments.

48. eConsent: The Missing Ingredient To More Engaging Clinical Trials 8/29/2022

    Electronic consent promotes better trial experiences, but many sites and sponsors are wary of giving up paper-based processes. Consider their reasons for caution and how teams can prepare for the switch.

49. Deploy eConsent Around The World With Confidence 8/16/2022

    Explore an easy, secure way to deliver highly engaging, regulatory-compliant electronic consent for trials of all types with IQVIA Complete Consent.

50. Top 5 Reasons You Need IRT Expertise (Not Just Software) 7/11/2022

    Gain insight into why pharma companies generally seek IRT vendor relationships to ensure high-quality builds that meet their needs and avoid the potential pitfalls associated with RTSM.