Investigational New Drug (IND) Studies | Preclinical Development | Charles River

investigational new drug (IND) 

During the preclinical stage of drug development, timelines are critical for the filing of an Investigational New Drug (IND) application within a predetermined timeframe and budget. Evolving market pressures have changed the focus of the drug development industry, accelerating early phases further in order to create late-stage pipeline growth. Given these increasing pressures, understanding how and when to plan your preclinical IND-enabling program is an integral part of meeting specific milestones leading to on-time IND submission.

Learn through our years of experience, unique range of services and best-in-class expertise how we are best suited to help you successfully initiate and complete your IND-enabling program. With our ongoing efforts to improve upon our internal processes and continued focus on scientific excellence and guidance, we are pleased to announce the most cost-effective IND program for our clients.

For your IND guide and full access to our accelerated reporting timelines, including a full-size Gantt chart, please log in to The Source. If you are not a member of The Source, our new online scientific and educational information center, please click here to register.

Gantt chart

Related Information
Webinar Replay – Planning and Understanding Your IND Program (January 2012)

For more information about our preclinical capabilities, contact us at 1.877.CRIVER.1 (1.877.274.8371) or askcharlesriver@crl.com.

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The Source

For more information, contact us at:

1.877.CRIVER.1 (1.877.274.8371)
askcharlesriver@crl.com

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Scientist I Wilmington, MA
Manager International Tax Wilmington, MA

Charles River Laboratories, Inc.