Biometrics in 2025: What Sponsors Need to Know Now
Biometrics in 2025: What Sponsors Need to Know NowAs we navigate 2025, the biometrics landscape is undergoing transformative changes that sponsors must understand to maintain competitive advantage. From AI integration to regulatory pressures, here's what you need to know to prepare your clinical dev...
Avoiding Rework: How Intelligent Programming Saves Time in the Later Trial Phase
In clinical trials, rework caused by inconsistent data structures, programming errors, or non - compliance with regulatory standards may delay submissions and increase budgets. By adopting proactive programming strategies, SAS developers and data managers can optimize work processes, reduce revision...
Case Study: Scalable Programming Excellence with FSP
GCP ClinPlus Enhances Trial Delivery for a U.S.-Based Ophthalmology SponsorThe ChallengeDuring a critical phase of multiple ophthalmology trials, the sponsor faced fluctuating programming workloads driven by concurrent studies and accelerated timelines. Internal capacity was stretched, and hiring fu...
Case Study: Strategic Clinical Oversight Accelerates Oncology Approval
GCP ClinPlus Supports New Indication for Nasopharyngeal Cancer Therapy The ChallengeIn the fast-paced field of oncology drug development, the addition of a new indication often presents complex regulatory, operational, and scientific challenges. In late 2024, our sponsor sought to expand the approve...
Global Biometrics Excellence: A Decade-Long Partnership Driving Pharmaceutical Success
Executive SummaryGCP ClinPlus established a transformative decade-long partnership with a US biotech company, delivering comprehensive biostatistics and SAS programming capabilities that significantly enhanced the client's biometric operations. By strategically integrating teams across US and China ...