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Blog
Practical Strategies for ICH Q14 and Q2(R2) Compliance
Ken Phares demystifies ICH Q14 & Q2(R2) guidelines with practical strategies for analytical procedure development, risk-based method design, and lifecycle management.
Blog
How Clinic-Ready Manufacturing and Adaptive Clinical Trials Can Reduce Drug Development Timelines
Discover how clinic-ready manufacturing and adaptive clinical trials streamline drug development, prevent delays, conserve your resources, and ensure safety, compliance, and efficiency.
Blog
The Year in Review 2025
The 2025 Year in Review highlights 30 years of drug development expertise, key milestones, events, resources, and innovations shaping early-phase research.
Blog
First-Timer Perspectives on Attending the AALAS National Meeting, by Brandon Ossont and Jennifer Lakritz
Brandon Ossont and Jennifer Lakritz share their first AALAS experiences, exploring scientific insights, networking, and professional growth in lab animal science.
Blog
Reflections on the ACT Annual Meeting: Where Science Meets Connection
Julie Forget reflects on the ACT Annual Meeting, highlighting cutting-edge toxicology research, gene therapy trends, and the strong sense of scientific community.
Blog
Case Study: Applying Scientific Expertise to Optimize Complex Safety-Focused DDI Studies
Altasciences conducted two drug-drug interaction studies to evaluate a novel cardiovascular therapy’s safety with clopidogrel and warfarin, ensuring safe co-administration.
Blog
30 Years of Innovation in Drug Development: The Evolution of the Contract Research Organization
Explore 30 years of CRO evolution, from preclinical roots to integrated, flexible partnerships—and how Altasciences is shaping the future of drug development.
