More and more clinical trials fail to meet key targets. Declining patient recruitment, engagement and retention result in insufficient or low-quality data, causing delayed or unsuccessful market authorization. PVR’s agile capabilities enable end-to-end quick project design, focusing on patient centric services and real world data solutions that contribute to the clinical trial and market success.
PVR is an agile Clinical Research Organization providing high‑quality clinical trial services for both pharmaceuticals and medical devices.
We operate in strategically selected, high‑performing regions recognized for operational efficiency, strong investigator engagement, and accelerated patient recruitment. These capabilities are strengthened by a global partner network, local in‑country experts, and an integrated clinical trial logistics partner - together enabling seamless, end‑to‑end international trial execution.
PVR supports the full clinical development lifecycle, from study design and start‑up through trial conduct and closure. Our offering also includes patient‑centric engagement solutions, Expanded Access and Compassionate Use programs, as well as Market Access and Real‑World Evidence (RWE) services.While we bring deep expertise in advanced and innovative therapies, our capabilities cover a broad range of therapeutic areas and development stages.
Our team averages 16 years of global clinical research experience, combining scientific rigor, operational agility, and nuanced regional insight to help sponsors generate meaningful data and efficiently advance their products toward market approval.
