Full-Service Trial Management for Drugs, Devices & Biologics
We specialize in large-scale studies and post-approval trials, with full-service delivery from site startup to study closeout.
Clinical Trial Management Services
PiVOT delivers end-to-end clinical trial management for drugs and devices, from early feasibility to large-scale Phase III and IV studies.
Drug and Device Trial Management
At PiVOT, our strength lies in executing pivotal Phase III trials and rigorous post-marketing (Phase IV) studies in the Philippines. We bring operational excellence, regulatory fluency, and deep local insight to each engagement, ensuring quality data, timely recruitment, and global compliance.
CORE CAPABILITIES:
Full-service trial execution from startup to closeout
Regulatory affairs, clinical monitoring, data management, and statistical analysis
Trial designs tailored for publication or regulatory submission
Full compliance with ICH-GCP, data privacy laws, and country-specific regulations
Post-Marketing Surveillance (PMS) & Real-World Evidence (RWE)
We support sponsors in demonstrating long-term safety and real-world value through end-to-end PMS and RWE management, covering everything from regulatory startup to final reporting.
OUR SERVICES INCLUDE:
Lifecycle management of PMS and RWE studies
Protocol development, site oversight, data analysis, and reporting
Compliance with GCP, privacy standards, and local regulatory requirements