Expanded Digital Resources

From our live and on-demand webinars, online learning through Charles River Campus, and scientific posters, our resources are here to guide 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.

coronavirus disease, also known as COVID-19

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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.

eGuide: Investigational New Drug (IND) Development Programs
eGuide: Standard for Exchange of Nonclinical Data (SEND)
Posters: Society of Toxicology (SOT) Resource Center – Access our 40 ePosters
Webinar | March 25, 2020: Interchangeability of Southeast Asian Sourced Large Animals and Managing Supply
Webinar | April 8, 2020: Mastering qPCR for Biodistribution and Shedding Studies of Cell & Gene Therapies
Webinar, On Demand: Succeeding with New SEND Requirements: Expert Panel Discussion
Webinar, On Demand: Unpacking the ERA Guideline Revisions
Webinar Series: Are You Ready for the Digital Pathology Revolution?

 

Laboratory sciences is an integral part of drug development, from the earliest stages of nonclinical work, requiring the efficient development and transfer of methods, to produce detailed, on-time data to support decision making. Access the latest resources to stay up-to-date on ADME, metabolites, and the microbiome.

Poster: Using Statistical Analyses to Demonstrate Equivalency Between Automated and Manual Processes to Deliver High Quality In Vitro ADME Data Even Faster
Video: Tackling Program Challenges in Cellular Therapy Research and Development
Webinar, On Demand: Enabling DMPK Science: Delivering In Vitro ADME Data “Even Faster”
Webinar, On Demand: The Therapeutic Axis of Microbiome, Inflammation, and Immune Response

 

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.

eGuide: Building a Biologic
Poster: A Comparative Analysis of Viral Clearance by Affinity and AEX Chromatography
Webinar | March 26, 2020: Choosing the Right Virus for Your Viral Clearance Studies
Webinar, On Demand: Analytical Techniques for Identification and Quantification of Process Residuals
Webinar, On Demand: Applying Next Generation Sequencing to Biologics Testing: What You Really Need to Know
Webinar, On Demand: Determining the Optimal Pyrogenicity Testing Approach for Your Product
Webinar, On Demand: Development, Validation, and Implementation of GMP Release Potency Assays for Vaccines
Webinar, On Demand: Endotoxin Testing Limits, Method Development and Validation for Plasma-Derived Products
Webinar, On Demand: LER: A Biopharmaceutical Operational Reality Perspective
Webinar, On Demand: New Strategies for Quality Control of Host Cell Protein Impurities