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Medical Device Registration Services Available In Usa Rhode Island

5 services found
Available In Rhode IslandNear Rhode Island

Medical Device Registration Services

Medical Device Registration Services

by:Emergo by UL   based inAustin, TEXAS (USA)
Commercializing your medical device first requires you to obtain registration and approval from regulatory agencies in each country where you plan to sell your device. Device registration requirements can vary significantly from country to country, which can create compliance challenges for ...
CONTACT SUPPLIER

Medical Device Regulation Compliance Services

Medical Device Regulation Compliance Services

by:Chemical Inspection & Regulation Service Limited (CIRS)   based inHangzhou, CHINA
Medical Devices and In Vitro Diagnostics Product Regulatory Compliance in China. Pre-market Investigation & Analysis. Medical Devices Registration & Approval. Clinical Trial Consulting. Manufacturing and Distributing License Approval. ...
CONTACT SUPPLIER

Consulting Services

Consulting Services

Manufactured by:Integrated Diagnostics Group, A division of Sanzay Corporation   based inMiami Gardens, FLORIDA (USA)
IDG helps you approach the medical device market with ease of mind. We assist you with Medical Device and IVD Registration, local in-country representation, distributor qualification and quality system ...
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Post-Market Surveillance Services

Post-Market Surveillance Services

by:Emergo by UL   based inAustin, TEXAS (USA)
Regulators in most medical device markets require registrants to meet post-market surveillance (PMS) obligations to maintain compliance. However, PMS rules can vary between different medical device markets, requiring manufacturers to develop tailored rather than one-size-fits-all approaches. With deep expertise ...
CONTACT SUPPLIER

Medical Device Services

Medical Device Services

by:HingeClinica   based inPrinceton, NEW JERSEY (USA)
HingeClinica is a world class partner for Medical Device services. We render End to End Medical device MDR compliance and Regulatory services, Clinical trial, Pharmacovigilance services to Medical Devices industry. Our Medical Device team has extensive experience in working with US FDA, EMA, PDMA, SFDA, Health Canada, DCGI and ROW, regulatory Submissions and ...
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