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Resources

Designed to inform you of the latest developments in our service portfolio as well as discuss specific technologies and regulatory issues of our industry.

IND eGuide

Download our IND eGuide to understand how and when to plan your preclinical
IND-enabling program as an integral part of meeting specific milestones necessary to timely
and efficient IND submission.

Navigating the Immunogenicity Guideline

The Draft 2016 Immunogenicity Guidance may not be final, but even its preliminary changes may affect your development program. Join our webinar to learn the best ways to plan your immunogenicity assessments during the preclinical and clinical phases of development.

Developing a Vaccine?

We’ve got you covered.

Today’s vaccines are increasingly complex; the sooner you get started, the better. See what your milestones timetable might look like with our new IND Gantt chart for vaccines.

 

Common Rodent Health Conditions Poster

A new tool for quickly identifying and addressing Health Issues

Unlock Our Historical Control Data

We’ve compiled comprehensive reproductive, developmental and juvenile toxicology historical control data on many of our research animal models. Access it through our exclusive content portal,  The Source℠.

How Much Test Article Does

Your Oral Gavage Study Require?

Eliminate waste, and ensure you have enough test article for dosing your tox studies with our interactive calculator. Just input your study details, and we’ll tell you what you need to plan for this important aspect of your program.

SEND eGuide

Recently updated, this resource covers key aspects of CDISC SEND and its effect on IND submissions to the FDA starting December 2017.

Embarking on an IND Journey?

This interactive tool is meant to provide you with an estimated timeline to help you better plan your IND program.

© 2018 Charles River Laboratories International, Inc.