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True Quality is a conference designed specifically for executives, quality, and regulatory professionals at high-performing medical device companies. The conference is also recommended for consultants, investors, and service providers. It is where the industry comes together to learn, network, and find inspiration.
True Quality is ideal for any industry representative at a MedTech company who is or intends to pursue commercialization in the U.S. & EU markets.
Learn, connect, and find inspiration at the must-attend experience for MedTech professionals, who drive ceaseless innovations in the market, today.
Listen and get inspired by the sessions like overcoming the barriers to improved quality, the new era of MedTech, mindset tools for high performance teams, etc.
Greenlight Guru is a modern quality management software platform built exclusively for the unique needs of the medical device industry.
Rightpoint, a Genpact company (NYSE: G) is a global experience leader. Over 700 employees across 12 offices work with clients end-to-end, from defining and enabling vision, to ensuring ongoing market relevance.
Globiox was founded on the principles of innovation, efficiency, and results. With 20 years experience in the life sciences industry, Patti Rossman started Globiox to deliver high-value life sciences consulting.
The only Electronic Data Capture (EDC) platform designed for Medical Devices & Diagnostics.
Nelson Labs, a Sotera Health company, is the industry-leading provider of global lab testing and expert consulting services. We perform microbiological and analytical laboratory tests across the medical device, pharmaceutical, and tissue industries.
ICS combines intuitive user experience (UX) design and world-class software development expertise with full product realization services around embedded, desktop and IoT applications to create transformative products for a connected world.
Proxima works with the new class of rising stars in drugs, diagnostics, devices and digital health. We help emerging companies overcome regulatory and clinical obstacles to get their medical product approved.
MedEnvoy is an independent Importer that supports manufacturers of Medical Devices and IVDs to meet Article 13 of the EU MDR and IVDR while maintaining full commercial control, independence, and flexibility.
Over the past 24 years, Life Science Outsourcing has partnered with more than 1,400 medical device innovators to streamline production and navigate complex regulatory landscapes.
Healthcare relies on regulatory product data submissions for quality, safety, reliability and transparency, benefitting the entire supply chain. Reed Tech is proud to play a role as a technology partner.
Kapstone Medical partners with physician inventors and manufacturers to develop and commercialize new medical devices. We do this by providing services for design, prototyping, patenting, quality systems, and regulatory approvals.
Compliance Solutions has many years of experience within the Life Science Industry (including Blood Establishments) in advising on how to best meet the regulatory requirements of the MHRA, FDA, Notified Bodies and ICH, for the one man start up to the
HSD, a SteriPack Company, is an ISO 13485-2106 certified product design and development firm specializing in medical, scientific, consumer healthcare products and packaging delivery systems.
A Secure, Compliant, Cost-Effective Cloud Solution for Medical Device Connectivity Compliant medical device connectivity infrastructure can be very costly and time consuming to build, operate, and maintain.
Velentium is a professional engineering firm, specializing in the design and manufacturing of therapeutic and diagnostic active medical devices.
Rook Quality Systems is a consulting firm dedicated to helping early-stage medical device companies develop and maintain effective and efficient quality systems.
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