Insights On Partnering
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The Tax Reporting Threshold Just Went from $600 to $2K — What to Know
7/22/2025
Explore the implications of the newly enacted "One Big Beautiful Bill" and how it will alleviate the administrative burdens faced by clinical research stakeholders and benefit low-income patients.
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When Should You Rescue Your Clinical Trial From A Bad RTSM?
4/28/2026
Stop settling for tech delays that drain your team. Learn how to evaluate a mid-study transition and implement a rescue plan that restores efficiency and control to your clinical operations.
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Ensure The Safe And Efficient Development Of High Potent Drug Products
8/16/2025
As your product transitions from clinical phases to commercial launch, flexible, globally compliant facilities stand ready to adapt to your evolving needs.
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Building Bioanalysis Infrastructure For Modern Drug Development
10/20/2025
Drug development accelerates with AI, decentralized trials, and adaptive protocols, but legacy CRO infrastructure lags. Platform-based systems enable speed, quality, automation, and continuous improvement.
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Two Views Of Risk When Choosing An IRT/RTSM Software Partner
5/5/2026
In this clip, Ryan Keane of Korio explains why legacy RTSM vendors, designed for large pharmaceutical companies, often struggle to serve smaller, fast-moving Sponsors.
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Medable's Japanese Clinical Trial Exceeds FPI Date And eCOA Adherence
3/10/2025
A top-10 global pharma company aimed to address eCOA adherence and patient enrollment challenges faced by clinical trial sites in Japan. Explore an initiative to enhance the patient and site experience.
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Case Management Accelerates Shipment For SCN1A+ Dravet Syndrome Gene Therapy
3/12/2026
Consider this streamlined, end-to-end solution that helped safeguard study timelines and ensured that patients with urgent medical needs could receive treatment without delay.
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Debunking 5 Misconceptions About Community-Based Research Sites
5/28/2025
By confronting misconceptions about community-based research, we uncover evidence of how sites effectively manage complex trials while maintaining high standards of care.
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Accelerator™ Drug Development 360° CDMO And CRO Solutions
3/4/2026
Review this coordinated suite of integrated solutions that brings together CDMO and CRO capabilities across clinical research, manufacturing, and clinical supply.
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PCI Capacity Update July 2025: Small Molecule Drug Product/Finished Dosage Form
7/29/2025
Dr. Rebecca Coutts highlights PCI’s high potent oral solid dose (OSD) and oral liquid capabilities, focusing on site expertise, specialized infrastructure, and handling of complex molecules.