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Medical devices of all classes, active implantable devices and procedure packs and kits sold in Italy to the Public Sector must be registered in an Italian database ("Repertorio"), administered by the Ministry of Health through its new system, NSIS.

Medical devices of all classes, active implantable devices and procedure packs and kits sold in Italy to the Public Sector must be registered in an Italian database ("Repertorio"), administered by the Ministry of Health through its new system, NSIS.

Arazy Group US company is Medes USA Inc., located in Seattle, Washington. Medes USA is a qualified and a recognized Regulatory Designated Agent.

Arazy Group US company is Medes USA Inc., located in Seattle, Washington. Medes USA is a qualified and a recognized Regulatory Designated Agent. We have been serving hundreds of companies worldwide since the new FDA regulation came into force on April 2002.

Arazygroup.com - Services in Argentina include in Argentina medical devices are regulated by The National Administration of Drugs, Food and Medical Technology (ANMAT) under the Ministry of Health. Medical products whether they are manufactured or imp.

Arazy Group experts can write the clinical literature review for your product based on the existing publications and your clinical studies while complying with both the international harmonized standards and the national guidelines.