Preclinical Resource Library

A Wealth of Information at Your Fingertips

Altasciences has an extensive understanding and decades of experience in IND/NDA-enabling toxicology, safety pharmacology, and laboratory services that meet global regulatory requirements.

Here are some of our most insightful scientific resources in preclinical development to guide you through every step of the journey:

• Webinars that cover topics related to the potential of miniature swine in preclinical studies, insights for avoiding common pitfalls in early drug development, and effective interpretation of toxicity data for classification.
  • Downsized Miniature Swine: A New Spin on the Oldest Model
  • Navigating the Challenges of Early Drug Development—How to Avoid Common Pitfalls
  • Case Studies Adversity Level Determination in Nonclinical Toxicity Studies
• ​​​​​​The Altascientist — A Scientific Journal that offers insights into the evolving role of miniature swine in preclinical safety studies, effective safety pharmacology practices, and valuable tips for planning successful preclinical assessments to support regulatory submissions.
  • A Changing Paradigm for Non-rodent Species in Nonclinical Safety Studies
  • Safety Pharmacology Studies - a Review
  • Navigating the IND Submission Process
• eBooks that help you navigate the preclinical regulatory process, identify key milestones for accelerated drug development, and delve into dermal testing solutions.
  • Nonclinical Assessment Planning Guide
  • Scratching the Surface of Dermal Testing

VISIT THE FULL LIBRARY

Speak with an expert today to learn more about our preclinical solution.

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Preclinical Services
Miniature Swine in Nonclinical Studies