Comprehensive certification process further validates Alveo as a trusted partner in the highly regulated healthcare industry, advances commercialization and partner opportunities globally
ALAMEDA, Calif.--(BUSINESS WIRE)-- Alveo Technologies, Inc. (Alveo), a leader in molecular sensing and diagnostics with its proprietary be.well™ technology platform, today announced its quality management system (QMS) has achieved ISO 13485:2016 certification for the design, development and manufacture of in vitro diagnostic kits and analyzers for the detection of infectious disease.
The globally recognized ISO 13485 standard, published by the International Standards Organization, sets out requirements for establishing and maintaining quality management systems for the medical device industry.
Compliance with the ISO 13485 standard is required for companies to market medical devices in many markets, including the European Union, Canada, Japan, and Australia. In addition, the U.S. Food and Drug Administration has announced plans to harmonize its existing medical device QMS requirements with ISO 13485, proposing new regulations that incorporate ISO 13485 as the foundational requirements.
“We are thrilled to achieve ISO 13485 certification,” says Alveo CEO Shaun Holt. “This official recognition from our notified body confirms that Alveo Technologies has developed a state-of-the-art quality management system that consistently delivers highly sensitive and specific molecular sensing and diagnostic results. We are committed to maintaining this standard and driving quality for our customers and partners.”
“I would like to emphasize that this is more than a piece of paper – it is proof positive to the world that our intense focus on quality has been independently verified,” Holt says. “Moreover, this assures current and future partners in agriculture, veterinary sciences, and aquaculture that we bring a high level of quality to their projects, their markets, and customers. ”
Alveo has developed a rapid, handheld, eco-friendly, multiplexed platform that pairs advanced molecular assays with cloud-enabled data analytics for real-time disease, pathogen and contaminant detection, analysis, and diagnosis. This mobile molecular lab is capable of delivering rapid testing at the point of need, for example, in doctor’s offices for various infectious diseases, in the field for crop testing, or on farms for livestock testing. Alveo is leading the transformation of the point-of-need molecular sensing and health tech markets with an open-platform approach to co-developing rapid molecular testing capabilities with collaborative partners across multiple markets. Initially focused on COVID-19 testing, the company has commercialized its be.well™ COVID-19 Test in the European Union, Middle East, and the Caribbean on the back of this certification.
Alveo’s conformity assessment was performed by GMED-LNE, a highly regarded French notified body globally renowned for its expertise in assessing medical device quality management systems for conformance to the standard. GMED (CE 0459) is designated as a Notified Body under Regulation (EU) 2017/746 and is one of only a few authorized to provide certification services to manufacturers according to Regulation (EU) 2017/746 (IVDR).
“This certification from GMED, one of the world’s most respected notified bodies, confirms that we have a top-notch quality management system for the design and development of compliant IVD products,” says Kevin Gunning, Vice President of Quality at Alveo. “In executing against our development pipeline, our QMS processes give us a high degree of confidence that the products we manufacture will continually meet customer expectations and regulatory requirements.”
About Alveo
At Alveo we understand the importance of access to cutting-edge molecular testing and cloud-based data analytics for rapid diagnosis and management of infectious diseases and other pathogens. With an initial focus on acute respiratory infections including COVID-19, Flu A/B and RSV, Alveo’s agile and dynamic molecular sensing and diagnostic platform, be.well™, can be adapted to detect a wide range of diseases, bacteria, and other pathogens that threaten public health, across all modalities. We believe increased access to real-time test results will transform the way individuals, healthcare providers and public health professionals identify and manage pathogens in humans, animals, plants, water, and beyond. With be.well™, we will Know Sooner, Act Faster™.
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