A patient-friendly informed consent form (ICF) is a key element for prospective clinical trial participants’ understanding of a clinical research study. In this blog, we delve into tips to ensure the ICF is clear and understandable. The research ICF document provides potential participants with the…
Retaining participants in studies is an ongoing challenge that the clinical trials industry grapples with daily. One analysis1 I came across pegged the participant dropout rate at an average of 25-26 percent per study. Every single loss is costly and, among other problems, can prolong…
Realistic, well-managed clinical trial timelines are essential to the success and timeliness of clinical studies. Read on for more information about keeping your projects on track. We often say every clinical trial is made up of a million moving parts. The materials, equipment, and supplies…
Whether you’re a sponsor, CRO, or part of a study team, writing clinical study materials that resonate with your audience is crucial for recruitment, referrals, and retention. Our tips will get you started and guide you through the writing process. You know all the standard…
Ancillary trial supplies and equipment play an essential role in most clinical trials. Selecting, procuring, and shipping ancillary supplies and equipment is a specialty that sponsors and CRO companies may find best to outsource. However, outsourcing is not as simple as selecting a vendor and…