Archives: Resources
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.
Biotech Product Launch Success with Medical Information
Discover how proactive medical information helps biotech teams avoid launch risks and ensure success.
US Inflation Reduction Act: Drug Pricing & Health Equity
Explore how the US Inflation Reduction Act is reshaping drug pricing, value-based care, and health equity.
Designing a lab for the new generation of biological therapies
Our GMP lab in Athalone, Ireland features a dedicated room for controlled temperature and humidity testing of inhaled biologics.
The Time Is Now for New Biosafety Testing Services
Thermo Fisher Scientific highlights the need to test for mycoplasmas and replication-competent viruses
How AI, Automation, and FSP Partners Are Reshaping Global Pharmacovigilance
Learn how AI-powered automation is streamlining pharmacovigilance case processing, reducing barriers, and helping sponsors scale safety operations efficiently.
Biomarker Capabilities Overview
Our biomarker lab works closely with customers to shape biomarker strategy and drive projects to completion, even where regulatory uncertainty exists.