At Parameters Research Laboratory, we are committed to providing comprehensive and high-quality services to our valued customers. Our key deliverables encompass a range of essential components to ensure the success and integrity of your clinical research projects. We follow Good Clinical Practice guidelines to ensure participant safety. We have a comprehensive Quality Management System to ensure compliance with requirements necessary while conducting Clinical Trials involving your Investigational Device. We help design study protocols in collaboration with our clients, submit the study documents for IRB approval, provide monitoring services during and after study execution, control the data management, provide data and physical lab security measures, as well as data analysis for a final study report.
SPONSOR SERVICES
STUDIES
BLOOD PRESSURE CLINICAL TRIALS
Whether you are conducting early-phase feasibility studies or large-scale clinical trials, our experienced team can provide end-to-end support. From protocol development to participant recruitment, data collection, and analysis, we ensure that your study is conducted with the highest standards of quality and compliance. Our state-of-the-art equipment and skilled personnel enable us to perform accurate and reliable blood pressure measurements in various test settings.
01
Arterial Line BP as reference:
Our team consists of highly skilled medical professionals, including physician anesthesiologists, research nurse clinicians, and technicians, who are experienced in conducting clinical trials on medical devices using arterial lines as the reference standard. Our Principal Investigator and Medical Director is a board-certified anesthesiologist who has placed over 1,700 arterial lines over the past two years for clinical trials. We have conducted numerous studies in Clinical Research Trials for development and validation of medical and wearable devices while using arterial line blood pressure as the gold standard reference. We utilize additional proprietary techniques in arterial line management to ensure accurate and reliable measurements of blood pressure. We understand that each research or clinical project is unique, and we will work closely with you to develop a study protocol tailored to your specific objectives and requirements.
02
Auscultatory BP as reference:
Our team of experts have years of clinical and research experience in medical device studies using Dual Auscultatory blood pressure measurements as the gold standard reference. Basing our protocol development on established blood pressure testing standards, we follow Good Clinical Practice to ensure that study conduct is performed according to the study protocol and that your objectives for development and validation of your blood pressure device is met. Our staff of fully qualified research clinicians have been fully trained on assuring accurate auscultatory blood pressure measurements. Our Quality management systems, security systems, and study monitoring services provides confidence that our data is accurate and reliable.
HUMAN FACTOR STUDIES
We conduct human factor studies which involves the scientific understanding of interactions between humans and devices. In healthcare settings, human factor studies help optimize and develop equipment design to improve clinical outcomes, and to ensure patient safety and the efficacy for use by intended users.
OTHER VITAL SIGNS PARAMETER STUDIES
While we currently specialize in Blood Pressure studies, we also have experience in development and validation studies for Respiratory Rate, Heart Rate and Pulse Rate, and Atrial Fibrillation/PVCs detection in EKG readings. As we continue to grow and expand, we plan to offer testing on all vital sign parameters.
Get in Touch
Would you like to partner with us? Discuss study development? Need a CRO? Submit the form below and our Principal Investigator will reach out to you to begin the conversation!