Online/Digital Education | Charles River Laboratories.

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Basic Research
Discovery
Safety Assessment
Laboratory Sciences
Biologics
Microbial

Basic research is the foundation of all scientific breakthroughs, improving our understanding of biology and advancing our knowledge of the life sciences. Learn more about our animal models and CRISPR technology.

Though rewarding, drug discovery can be a challenging journey. Too often, a novel compound’s road to market is delayed – or blocked entirely – by limited resources or expertise. Learn how to mitigate those delays through our approach to target discovery, hit finding, lead optimization, and beyond.

EGUIDE

Hit-Finding – A Walk-Through of HIT ID Approaches and Next Steps

POSTERS

High Content Analysis of 2D and 3D Cellular Models for Target and Phenotypic Drug Discovery

Molecular and Functional Characterization of Stem Cells-Derived Glutamatergic Neurons in Support of Drug Discovery Applications

Rapid Antibody Discovery on Hard Targets Combined with Fine-Grained Engineering and Optimization

Tools for Identifying and Monitoring PD Immune Biomarkers from Pre-Clinical Through to Clinical Stages of Drug Discovery

VIDEO SERIES

Charles River Presents: The Neuroinflammation Symposium

WEBINARS

Bioinformatics: Mining Big Data to Discovery Precision Oncology Therapies

The Therapeutic Axis of Microbiome, Inflammation, and Immune Response

A Translational Approach to Monitoring Batten Disease

When Immune Cells Invade a Tumor: Using the TME to Drive Your Oncology Research

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.

EGUIDES

Investigational New Drug (IND) Development Programs

Standard for Exchange of Nonclinical Data (SEND)

POSTERS

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

WEBINARS

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

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.

EPOSTER PRESENTATIONS

Quantification of mRNA Expression Using DNA-based Standard Curve RT-qPCR Methods

Validation of an LC-MS/MS Assay To Measure Arginine, α-k-δ-GVA, Argininic Acid, Guanidinoacetic Acid, and Nα Acetyl-L-Arginine Concentrations in ARG1-D Patients ePoster

POSTER

Using Statistical Analyses to Demonstrate Equivalency Between Automated and Manual Processes to Deliver High Quality In Vitro ADME Data Even Faster

Is complement C3 a valuable marker for the activation of the complement cascade?

Sensitive Detection of Human Cells in Murine Organ DNA by qPCR

VIDEO

Tackling Program Challenges in Cellular Therapy Research and Development

WEBINARS

Enabling DMPK Science: Delivering In Vitro ADME Data “Even Faster”

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.

EPOSTER PRESENTATIONS

ASGCT Meeting Resources – Access our ePosters

POSTERS

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

WEBINARS

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

Testing for microbial contaminants is necessary to ensure the safety and quality of their products, but the process can add costly delays in their release to market. Learn how to streamline testing and mitigate these risks with revolutionary technologies and exceptional services that have changed the way the industries conduct quality control. See a more comprehensive list here.