Blogs
GLP-1 Clinical Trials: 5 Key Strategies and 5 Pitfalls to Avoid
Success in GLP-1 clinical trials requires a balanced approach that combines innovative strategies with careful attention to potential pitfalls. As sponsors navigate this growing pharmacological…
ICH E6(R3) Good Clinical Practice: Modernizing Clinical Trials and Aligning with YPrime’s Innovations
The International Council for Harmonisation of Technical Requirements for Human Use (ICH) issued the E6(R3) Good Clinical Practice Guideline on January 6, 2025. It updates…
Evaluating eCOA Options for Oncology Clinical Trials
The integration of connected devices in clinical trials enhances clinical research, elevating data collection, patient engagement, and overall study efficiency.
AI in Clinical Trials—The FDA’s New Draft Guidance
AI in Clinical Trials—The FDA’s New Draft Guidance A YPrime Blog By: Shawn Blackburn,Founder, YPrime On January 6, 2025, the FDA released a landmark draft…
Can Paper COA Deliver ALCOA?
With vulnerabilities like human error, ambiguous entries, and delayed documentation, paper COA falls short. Enter electronic clinical outcome assessments (eCOAs)—the only COA solution that not…
Connected Devices in Clinical Trials: Adoption Continues to Advance
The integration of connected devices in clinical trials enhances clinical research, elevating data collection, patient engagement, and overall study efficiency.
YPrime’s Commitment to the UN Global Compact
YPrime’s Commitment to the UN Global Compact—A Letter From Our CEO, Jim Corrigan A YPrime Blog By: Jim Corrigan,Chief Executive Officer, YPrime YPrime’s Commitment to…
YPrime 2025 “Year in Preview”
In this forward-looking analysis, six (6) YPrime subject matter experts offer their unique insights into the priorities shaping the future of clinical trials.
Properly Scoping eCOA Projects—A Critical Success Factor in Clinical Trials
Successful eCOA implementation requires thorough protocol review and deep operational insight.
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