Expanded Digital Resources

From electronic files of our scientific posters and live and on-demand webinars to online training and learning through the Charles River Campus website, our digital resources are here to educate you along every step of the drug development pathway. Check out the latest resources to keep you up-to-date with industry hot topics and the latest research. Can't find the information you're after?
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Determination of a drug’s safety profile is perhaps one of the most critical stages of the drug development pathway. Complications and inefficiencies at this late phase of the journey can create costly delays. See the latest resources to help you overcome these common issues.


Investigational New Drug (IND) Development Programs
Standard for Exchange of Nonclinical Data (SEND)


Society of Toxicology (SOT) Meeting Resources – Access our 40 ePosters


Are You Ready for the Digital Pathology Revolution?
Interchangeability of Southeast Asian Sourced Large Animals and Managing Supply (Available through The Source℠)
Succeeding with New SEND Requirements: Expert Panel Discussion
Unpacking the ERA Guideline Revisions


The approval process for ensuring the identity, potency, purity, safety, and effectiveness of a biopharmaceutical is complex. Navigating this process effectively is critical to the ultimate commercial success of a product. Find out more about building your biologic, viral clearance, next generation sequencing and more with our array of digital resources.


ASGCT Meeting Resources – Access our ePosters


Considerations for the Use of AUC for Characterization and QC Testing of AAV Gene Delivery
A Platform Approach for Analytical Methods to Support Adeno-Associated Virus (AAV) Gene Therapy Products


Advanced Mass Spectrometry-Based Characterization of Adeno-Associated Viruses and Next Generation Biologics
Analytical Ultracentrifugation for Characterization of AAV Gene Delivery Vectors
A Platform Approach for Analytical Methods to Support Adeno-Associated Virus (AAV) Gene Therapy Products
Viral Clearance Challenges for Gene Therapy Products