Preclinical and Chemistry, Manufacturing, and Controls (CMC)
Expertise and guidance to create a solid foundation that supports your successful preclinical submissions
We provide comprehensive Nonclinical and Chemistry, Manufacturing, and Controls (CMC) services designed to advance your drug development program efficiently and effectively. Our Nonclinical A-team and CMC experts provide strategic guidance and support throughout your preclinical phase, ensuring a solid foundation for your IND, IMPD, or IDE submission and subsequent clinical trials.
Preclinical Development
Our nonclinical experts will help design tailored preclinical development programs that meet regulatory requirements in the most cost-effective and time-efficient manner without compromising the quality of the overall safety assessment.
Chemistry, Manufacturing and Controls
Our comprehensive experience in the industry enables us to ensure that your CMC program has the requisite quality, consistency, and technical validity while conforming to the various global regulatory requirements and quality standards.