Medical Device Clinical Trial Manufacturers, Suppliers & Companies In USA
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Software vendorbased in Raleigh, NORTH CAROLINA (USA)
Ofni Systems, a private computer compliance services and software company, is headquartered in Research Triangle Park, NC. Ofni Systems was founded in 1999, dedicated to helping companies address the requirements of 21 CFR Part 11, Electronic ...
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Software vendorbased in Mountain View, CALIFORNIA (USA)
DNAnexus has built the world’s most secure cloud platform and global network for scientific collaboration and accelerated discovery. We embrace challenges and partnership to tackle the world’s most exciting opportunities in human health. We are ...
GXP Services
The xVantage Group helps customers with their medical device submissions, their clinical trial protocols and submissions, managing data collaboration from CROs, their regulated ...
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ManufacturerOffice in Houston, TEXAS (USA)
Chemical Inspection and Regulation Service (CIRS) is a leading product safety and chemical management consulting firm providing valued product regulatory compliance service, tailored solutions and original information to help our clients gain ...
Medical Device Regulation Compliance Services
Medical Devices and In Vitro Diagnostics Product Regulatory Compliance in China. Pre-market Investigation & Analysis. Medical Devices Registration & Approval. ...
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Technologybased in Princeton, NEW JERSEY (USA)
HingeClinica is founded and managed by a team of vast experienced clinical research professionals, medical and scientific experts to render the world class clinical research services to life sciences industry and to accelerate the research right ...
Medical Device Services
HingeClinica is a world class partner for Medical Device services. We render End to End Medical device MDR compliance and Regulatory services, Clinical ...
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Training providerbased in Palo Alto, CALIFORNIA (USA)
Enhancing global compliance, creating a world where quality and compliance professionals, regulators, and government agencies come together to help the world comply with the intent and the spirit of laws, policies and mandates, ensuring continuous ...
21CFR Part 11 and Harmonization with 21 CFR Part 812 for Medical Device Trials
Conducting clinical trials in a rapidly evolving electronic environment presents a unique challenge to the medical device industry where not only quality (GLP/GMP) plays an ...
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