Fast-Tracking
Life-Changing
Therapies
to market from concept
to IND and beyond
Fast Facts
Safety Assessment: No matter your endpoints,
we will help you reach them.
Benefits of working with a trusted partner with proven performance
~
INDs supported in last 12 months
+
IND programs per year
reports delivered last year, including non-GLP and GLP drafts—final and unaudited
Our Expertise at Your Service
Scientific Advisory Service – partners in your success
+
years of cumulative experience
+
years average experience per team member
+
scientific experts
Our track record of success
in supporting your needs
+
client and regulatory
agency inspections
per year
+
patents
28-day
toxicology studies
per year
%
SEND
datasets
accepted
Experience with a wide range of modalities
Small Molecule
Cell & Gene Therapy
Biologics
Vaccines
Chemical
Veterinary Pharmaceutical
Agrochemical & Biocide
Medical Device
Mitigate risk and meet your milestones in record time with a multidisciplinary, integrated approach to development. From full regulatory programs and specialty studies to analytical support and SEND, you’ll find everything you need to plan, execute, and submit a successful IND application at Charles River.
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