Archives: Resources
Success from Day One: How Emerging Biotechs Maximize the First 120 Days
Learn how emerging biotechs can optimize the first 120 days of clinical trials with smart planning, coordination, and communication.
Clinical Trials Evolve: Mixed FSP/FSO Models Add Agility and Expertise
Learn how mixed FSP/FSO models combine expertise and CRO scale to accelerate clinical trials.
How ICH Oversight Changes and AI Are Shaping the Future of Clinical Trials
Discover how ICH E6 (R3) reshapes trial oversight and how AI shows predictive insights, automated analytics, and unified platforms boosts compliance.
Overcome the complexity of drug development
Discover how to overcome clinical trial complexity with strategies that streamline operations, reduce risk, and improve drug development efficiency.
FSP 30 years advantage – Pharma’s Almanac
Learn what advance has had the greatest impact on the industry over the past 30 years and why.
The Evolution of Precision Medicine in Age-Related Neurological Diseases
Learn how biomarkers and patient-centric strategies help advance treatment and trial design for older adults with neurological diseases.
Clinical Trial Quality Checklist
Explore a clinical trial quality checklist to spot gaps fast, reduce inspection risk, and keep your study audit-ready from day one.
How Mixing FSP and FSO Models Bring Agility to Modern Clinical Development
Discover how hybrid FSP/FSO models enhance flexibility, control and efficiency in clinical trials, reducing costs and accelerating development.
AI in Regulatory Medical Writing: Balancing Innovation with Human Expertise
Discover how AI enhances regulatory medical writing, boosting productivity and accuracy while keeping human expertise central.