Who We ServeMedical Devices Industry
How We Help the Med Device Industry
For regulatory professionals in medical device manufacturing and distribution organizations, Reed Tech serves almost half of the top thirty medical device manufacturers. With experience ranging from start-up manufacturers to mid-size and industry-leading manufacturers, Reed Tech understands the challenges and serves the call for that ‘last mile of support’ for compliance. We offer solutions that help facilitate the research, collection, analysis, transformation, and submission of regulatory data to Health Authorities (US FDA, EU MDR UDI, China NMPA and others.)
UDI data solutions for device makers
Submit your UDI data to regulatory Health Authorities with confidence.
Manufacturers & Consultants
Efficient research for 510(k)s
Find predicate and successor devices and simplify post-market surveillance.
Regulatory and Compliance
In Regulatory Affairs, having the latest information available concerning health authorities both at home and globally is key. Submission planning for FDA, EU and other global regulators requires end-to-end product data management processes. To provide forecasting, audits, and tracking of global change management, RA is depended upon to set the strategy for achieving compliance.
Investment in technology and strategic vendor relationships will ensure flawless execution for achieving supply chain goals.
Managing product data information for the medical device lifecycle is a multi-prong mission. Continuing efforts to simplify processes and create efficiencies for time and resources is paramount. When it comes to answering product data lifecycle challenges, Reed Tech can become a valuable extension of your team. In addition to specializing in ‘all things UDI’, Reed Tech provides a centralized, affordable platform allowing for product data traceability and control. Managing regulatory compliance and meeting deadlines is what we do every day.
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