CE Marking Consultants in France

Paris added on 05-09-2011, Classified number: 4662

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CE Marking Consultants in France
05-09-2011 Paris

Plan to foray into the medical device market in France? Get the all-important CE mark approval with the help of global leaders in medical device consultancy. Arazy Group offers authorized representative and helps medical device manufacturers and distributors get CE mark approval and market validation from the concerned medical device regulatory authorities through its services.

We offer clinical literature review and documentation services to fulfill the required norms and specifications for earning CE marking in France. After CE mark approval, get your medical devices registered with the local Ministry of Health in France. This way you can easily foray into the medical device market through our technical document preparation and CE Mark registration services on all medical devices, IVDs and equipment of domestic as well as overseas manufacturers.

We also offer Arazy Group unique line of GlobaR - Global Regulatory Hub (Trade Mark) products such as GlobaR Dossier (Trade Mark), GlobaR - One World Process (Trade Mark), GlobaR Submission Center (Trade Mark) and Universal Authorized Representative (Trade Mark).


For more information on our medical device consultants and regulatory services in France, feel free to contact us today!

Contact Details
Phone: +1 604.681.6888
E-mail: info@arazygroup.com
Website: http://www.arazygroup.com/medical_device_registration_in_france_

(Fill out our enquiry form on the website and reach us instantly or chat with us on our site)

Join us on Facebook: http://www.facebook.com/arazygroup

Follow us on Twitter: http://twitter.com/arazygroup

Connect with us on Linked In: http://www.linkedin.com/company/arazy-group

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