Clinical Trials: Trends to Watch For In Next 5 Years
Clinical trials are at the heart of medical innovation, driving the development of new treatments and therapies. As we look ahead to the next five years, several key trends are set to revolutionize the landscape of clinical trials. From technological advancements to regulatory changes, here’s a closer look at the biggest trends shaping the future […]
The Benefits of Implementing Digitized SoA in Clinical Research Protocols
The Schedule of Assessments (SoA) in clinical research protocols serves as one of the most important roadmaps clinicians, researchers, sponsors, and monitors use to guide the trial from start to finish. This roadmap, also sometimes referred to as the Schedule of Activities or the Schedule of Events, outlines study visits and scheduled activities expected for […]
Top 5 Technology Trends to Keep an Eye on in Clinical Research in 2024
There is no denying that technology is continually advancing year by year, month by month, and even day by day. As expected, this affects the scope of clinical research in 2024. While we learn to adapt and implement these technologies in our everyday lives, the clinical research field is working to capitalize upon these advancements […]
Digital Patient Engagement and Its Impact on a Digital Transformation of Life Sciences
What is Digital Patient Engagement (DPE) With greater emphasis on patient centricity, it’s increasingly important to engage with them in the digital landscape. Finding ways to meet patients where they are to better engage with and educated them through their entire care journey. Is digital data capture tied to patient-centric approaches for the design and […]
What the New FDA Guidance on Electronic Records and Signatures Means for Clinical Trials
The digital age is upon us. The FDA has acknowledged the increasing use of computerized systems to manage electronic records generated in the production of FDA-regulated products with applicable regulations and several guidance documents that strive to protect public health by securing digital data integrity. In March of 1997, the FDA released 21 CFR Part […]