Regulatory Affairs

Accelovance's Regulatory Strategy and IND Support team provides expertise and resources to help early stage clients bring products into clinical development. We support biologics, drugs, and medical devices with a comprehensive understanding of both regulatory and clinical affairs – blended knowledge that provides sound guidance for our clients. These individuals have over 20 years of experience coordinating pre-IND packages, INDs, IDEs, 510Ks, BLAs/NDAs/PMAs/MAAs, regulatory submission strategies, regulatory meeting preparation and attendance, and clinical trial launches. We have successfully supported US, EU, and Asia Sponsors in their US regulatory filings.

Contract Research Organization (CRO)

Accelovance is an award-winning, niche Contract Research Organization (CRO) focused primarily in oncology, vaccines, and general medicine.

Patient Recruitment

Accelovance blends conventional tactics with innovative ideas for a comprehensive strategy to find the RIGHT patient/subject for your study.

Clinical Call Center

As a patient-centric organization, Accelovance's Clinical Call Center uses clinically trained Call Center Agents who work seamlessly with clinical sites enrolling patients, Sponsors, and/or CROs.