PVCR has over 20 years of experience in the pharmaceutical industry, from drug discovery through clinical trials, including cGMP manufacturing, working with a diverse array of clients. Whether your goal is to bring a drug to market, raise capital, or position for acquisition, PVCR has the experience and capability to assist you.
PVCR can manage your clinical study from protocol creation through writing the clinical study report. We make sure your clinical program stays on-schedule and in-budget, while maintaining regulatory compliance and quality.
We provide IRB and TMF management services, audits, IND submissions, and more. PVCR can help make sure you comply with regulatory requirements.
Contact us as 1-888-440-3828 x 110 or click the button to send an email.