Learn
Cenduit Learn

white papers

White Paper: Drug Accountability & Returns Mgmt - DARM

It is time for our industry to move forward to bring drug accountability into the 21st century. The proven benefits include improved patient safety, enhanced RBM and quality, reduced site burden, reduced risk of inspection and audit findings as well as the ability to close out studies more quickly, thereby cutting costs. Additionally, since DARM functionality is already fully integrated into solutions that sites and sponsors are already using via the IRT system, the deployment and set-up efforts are minimal. Is your organization ready to benefit from electronic drug accountability?

Read More

IRT, Drug Accountability, White Papers

White Paper: Five Ways To Get More From Your IRT System

IRT is changing rapidly. Your needs and the solutions you employ to keep your studies on track need to do more than just keep up - they need to keep you out in front. Areas such as drug accountability & returns, forecasting, patient retention, integration and automated monitoring. All keys to the success of your trials . Learn more about each in this helpful tool.

Read More

IRT, Drug Accountability, White Papers

White Paper: Forecasting | Cenduit

Accurate forecasting of clinical supplies has become increasingly important in the past several years as planning the amount of study drug and other materials required to complete a trial has grown in complexity. Key drivers adding to this complexity include increased numbers of trials, reduced start-up timelines, patient recruitment challenges, globalization leading to more distant clinical sites and a variety of regulatory requirements, and escalating costs for investigational drugs and comparators.

Read More

IRT, White Papers

Unintentional Unblinding | White Paper | Cenduit

Maintaining the study blind is a critical part of maintaining the integrity and validity of any clinical trial. Experienced IRT providers have a variety of SOPs, system controls and well-trained members of staff to ensure that all blinded reports, data transfers and study documentation and communications are sanitized and free of any sorting or data that could even partially reveal the study medications in inventory or those assigned to patients.

Read More

IRT, Drug Accountability, White Papers

Trial Supply Management | White Paper | Cenduit

Managing clinical supplies effectively and efficiently requires a skillful blend of art and science to balance dozens of variables in order to create a fully optimized supply chain strategy.

Read More

IRT, White Papers

Modern Randomization Techniques | White Paper | Cenduit

Randomized, double-blind clinical trials are the gold standard for adequate and well-controlled studies in modern times. In this white paper, you'll learn how important randomization is, and how an effective randomization plan built into an IRT system forms the basis of a bias-free, well-controlled trial.

Read More

Randomization, White Papers

Electronic Drug Accountability Systems: | White Paper | Cenduit

The increase in federal audits and the growing federal regulations has made drug accountability management a major challenge. A failed federal audit leads to costly trial delays, and possibly non-approval or criminal liability. Electronic drug accountability managed through an IRT system can ensure compliance, reduce inefficiencies, preserve data integrity and increase patient safety.   

This white paper examines how electronic drug accountability managed through an IRT system:

  • Improves protocol compliance
  • Reduces clinical trial inefficiences
  • Preserves study data integrity
  • Increases patient safety
Read More

IRT, White Papers

Science of Patient Reminders | White Paper | Cenduit

The average cost of a patient lost to follow-up is $5,000. Download this paper to learn how to incorporate patient reminders into your protocol to reduce cost and resource wastage associated with patient noncompliance and early withdrawal.

Read More

Patient Reminders, White Papers