CLIENT PARTNERSHIPS AND TESTIMONIALS
We are proud to support a wide range of medical device innovators. While many of our partnerships remain confidential, the testimonials here offer a glimpse into the lasting business relationships we have made, the dedication to our work, and the quality we bring to every study.
"Thx Arthur Cabrera, MD and the entire Parameters Research Laboratory, Inc.. This wouldn't have been possible without your talent and dedication!" - Josep Sola, Co-founder, CTO, Hilo by Aktiia
"Midmark has collaborated with Parameters on several device-validation projects and has consistently been impressed by their professionalism. Each engagement has been completed on time and within budget, with clear and proactive communication at every step. The clinical rigor and expertise they bring give us complete confidence in the reliability of every study’s outcomes." -Thomas Schwieterman M.D., Chief Medical Officer and Vice President of Clinical Affairs, Midmark Corporation
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KehaAI, Inc.
INDUSTRY MEMBERSHIPS AND ENGAGEMENTS
Contributing to International Standards
Our Principal Investigator and Chief Medical Officer, Arthur Cabrera, MD, is actively involved in shaping the future of blood pressure monitoring through his participation on two international standards committees:
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ISO 81060-7, which focuses on the validation of cuffless, non-invasive blood pressure devices
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ISO 81060-3, the upcoming standard for continuous cuffless blood pressure measurement
Dr. Cabrera’s contributions help ensure that emerging technologies are held to rigorous standards for accuracy and reliability in both clinical and consumer settings.
Dr. Cabrera has been appointed as a U.S. expert to ISO/TC 121/SC 3/JWG 10, Oximeters, the international working group responsible for developing standards related to pulse oximetry equipment. In this role, Dr. Cabrera will contribute technical expertise to the drafting and review of international standards and will participate in national and international standardization activities. Serving in an individual expert capacity, Dr. Cabrera will collaborate with stakeholders worldwide to advance pulse oximeter safety, equity, and performance.
The AMA engaged with PRL to provide their expertise in the field of blood pressure device validation testing. PRL prepared guidance outlining the complexities of validation testing and clinical use of emerging technologies for cuffless blood pressure measurement to assist the AMA in assessing suitability of this technology for inclusion on the Validated Device ListingTM (VDL, validateBP.org)