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. Quality Assurance & Compliance. Risk Assessment & ...
By Chemical Inspection & Regulation Service Limited (CIRS) based in Hangzhou, CHINA.
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 ...
By Integrated Diagnostics Group, A division of Sanzay Corporation based in Miami Gardens, FLORIDA (USA).
The DM 21 December 2009 establishes the obligation to register in the medical devices database uses new methods. Registration is mandatory for all manufacturers and other entities responsible for placing devices on the Italian market for Class I, IIa, IIb and III, kits and assemblies and active implantable ...
By Endo Endoengineering Srl based in Falconara Marittima, ITALY.
The Food and Drug Administration (FDA) regulates all medical devices in the United States to make sure they are safe and effective. These regulations are a critical part of the medical device development process, and they will likely influence the design and testing of new medical devices. ...
By in2being, LLC based in Saline, MICHIGAN (USA).
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