WHY CLIENTS CHOOSE PRL
Specialized, Full-Time Research Team
Our dedicated on-site team comprises our Principal Investigator, Dr. Arthur Cabrera, clinical registered nurses, and research technicians (CRCs and CRAs), all of whom possess deep expertise in vital signs validation. This expertise provides continuity, technical precision, and rapid execution across all phases of your study.
Full-Service Clinical Research Organization (CRO)
PRL manages every aspect of your clinical validation study. From protocol design and regulatory strategy to participant recruitment, data collection, maintenance of essential documents, and submission-ready reporting. Our full-time, GCP-trained team ensures seamless execution, constant communication, timely study monitoring, and results that meet FDA, ISO, and international standards — all under one roof.
Leaders in Standards Development
As active contributors to ISO 81060-7 for cuffless blood pressure devices, PRL stays at the forefront of regulatory evolution, helping sponsors anticipate and align with future requirements.
Scalable, Multi-Site Capability
We offer operational flexibility to conduct studies across multiple locations with traveling clinical teams and regionally focused recruitment strategies. By using our specialized and experienced study teams for secondary investigational sites, we ensure consistent study execution and data integrity for your multi-site clinical trial.
Robust, Curated Participant Database
PRL’s robust, diverse, and comprehensive database enables targeted recruitment, including participants with specific medical conditions and demographics to meet study phenotype requirements.
Quality Assurance & Regulatory Compliance
Every study at PRL is backed by rigorous quality assurance processes and a deep understanding of regulatory requirements. We maintain meticulous documentation of essential documents, internal audits, and continuous oversight to always ensure data integrity and inspection readiness.
Collaborative, Partnership-Driven Approach
We prioritize long-term relationships built on open communication, technical collaboration, and a shared commitment to your product’s success.
Uncompromising Clinical Integrity
PRL operates under strict Good Clinical Practice (GCP) standards, ensuring every study meets the highest standards for quality, ethics, and regulatory compliance.
At PRL, we are deeply committed to honesty, integrity, and building lasting partnerships. Our goal is to work closely with you to support your objectives and contribute meaningfully to your success.