What Is CRF in Clinical Trials
What Is CRF in Clinical Trials – Reputable Health Studies Methodology Contact Book Strategy Call // REPUTABLE Studies Methodology Contact Book Strategy Call Methodology Spotlight What Is CRF in Clinical Trials Jul 20, 2025 12 min read Reputable Operations Team A Case Report Form (CRF) is a document used to collect data from participants in […]
What Is a Phase 2 Clinical Trial?
What Is a Phase 2 Clinical Trial? – Reputable Health Studies Methodology Contact Book Strategy Call // REPUTABLE Studies Methodology Contact Book Strategy Call Clinical Phases What Is a Phase 2 Clinical Trial? Jun 15, 2025 11 min read Reputable Analytics Team Phase 2 clinical trials are the second stage of testing a new human […]
How Long Do Clinical Trials Last with Wearable Tech?
How Long Do Clinical Trials Last with Wearable Tech? – Reputable Health Studies Methodology Contact Book Strategy Call // REPUTABLE Studies Methodology Contact Book Strategy Call Research Acceleration How Long Do Clinical Trials Last with Wearable Tech? Jun 15, 2025 14 min read Reputable Analytics Team Clinical trials are essential for developing new treatments and […]
Wearables in Clinical Trials: Pros and Cons
Wearables in Clinical Trials: Pros and Cons – Reputable Health Studies Methodology Contact Book Strategy Call // REPUTABLE Studies Methodology Contact Book Strategy Call Technology Review Wearables in Clinical Trials: Pros and Cons Jun 22, 2025 12 min read Reputable Analytics Team Wearables have revolutionized how clinical trials collect health data from participants. These devices […]
How Long Does It Take to Get IRB Approval for Health Wearable Tech?
Planning a health study using wearable technology? Find out how long it takes to get IRB approval and what influences the timeline. This comprehensive guide explains why IRB approval is essential for ethical research, participant safety, and data privacy in health wearable studies. Learn about the different levels of IRB review—from exempt studies taking 1-2 weeks to full board reviews that may take 4-8 weeks or longer. Get practical tips on preparing your IRB application, including detailed study design, data security measures, and consent documents, to minimize delays and ensure a smooth approval process. Understanding the IRB review timeline is crucial for effectively planning your study and enhancing the credibility of your research.
Are Clinical Trials Safe? (And Why Wearable Trials are Safest)
Wondering if clinical trials are safe? This comprehensive guide delves into the multiple layers of safety protocols in place—including IRBs, informed consent, DSMBs, and FDA oversight—to protect participants. Discover how wearable device trials take safety a step further by using non-invasive technology like smartwatches and fitness trackers for real-time health monitoring. Learn about the benefits of participating in wearable clinical trials, such as contributing to cutting-edge research, earning compensation, accessing personalized health insights, and experiencing lower risks compared to traditional drug trials. Find out how to join a wearable clinical trial and why it might be the safest and most rewarding option for you.