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Most foreign health authorities require a manufacturer to present a Certificate of Free Sales (CFS) from the country of origin or the European Union (EU) as part of the requirement for the medical devices import certificate in their territories.

Arazy Group, the global medical device consulting firm offers medical device registration in Lebanon to domestic as well as overseas medical device and equipment manufacturers. You can foray into the Lebanese market with your medical products after gaining market approval and clearance from the different medical and health regulatory bodies in Lebanon.

Arazy Group, the global medical device consulting firm offers medical device registration in Lebanon to domestic as well as overseas medical device and equipment manufacturers. You can foray into the Lebanese market with your medical products after gaining market approval and clearance from the different medical and health regulatory bodies in Lebanon.

Gain compliance with the Ministry of Health (MOH) in Jordan for your medical products with the aid of world leading medical device consultants. Arazy Group helps you introduce and foray into the Jordanian market with your medical devices and equipment like no other medical device consultant.

Gain compliance with the Ministry of Health (MOH) in Jordan for your medical products with the aid of world leading medical device consultants. Arazy Group helps you introduce and foray into the Jordanian market with your medical devices and equipment like no other medical device consultant.

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.

For medical devices cleared for sale with the USA - FDA, a Certificate for Foreign Governments (CFG) can be issued instead of a CFS. Select the "type of service required "available in the attached form for more information of CFG.

Medical device and IVD equipment manufacturers mostly operate within the boundaries of a quality system, which complies with one or more of the international harmonized standards. Those systems are subjected to audits as part of the certification process and regulatory compliance. Internal audits performed by external bodies are a great way to control and maintain QMS activities.

Arazy Group leading medical device consultants in Taiwan offering international standard in achieving market clearance and clinical review clearance for medical devices and equipment in Taiwan under the Taiwan Department of Health (DOH).

Arazy Group offer international standard solution in achieving and surpassing the verification and validation norms of different medical device and health regulatory bodies in China.

Medical Device specific regulation strategy reports, Medical Device Registration with PMDA, Japan Health Technical documents Preparation, Japan Market Authorized Holder and local Representative (MAH), Japan GMP compliance and Arazy Group's unique line of GlobaR - Global Regulatory Hub™ products.

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.

http://www.arazygroup.com - Ministry of Health clearance or MOH clearance throughout the Middle East, Africa and Asia for medical device registration and regulatory services.