Medical Device Registration in Lebanon

Regulatory authority: The two bodies regulating medical device registration in Lebanon are The Drug Import and Export Department and The Sanitary Engineering Service, which both act under the Ministry of Public Health.

Classification: The Lebanese authorities accept all classification systems. The type of product dictates the procedure it must undergo before receiving marketing authorization.

The process must be carried out by a local representative.

Timeframe of registration: Medical device registration in Lebanon requires a period of three months.

Length of license: The registration process is an import permit and must be performed with every shipment.

As of 2012, Arazy Group now offers our new service, LICENSALE.COM. This unique, cloud-based application provides you, the medical or IVD device manufacturer, with a comprehensive service that results in the successful registration of your product in Lebanon and ownership of the registration license through your company.

Once you register in Lebanon through LICENSALE.COM, a global compliance profile is generated that easily facilitates the registration of your product in more than 80 countries around the world. LICENSALE.COMcreates a foundation that makes registration simpler, faster, and more cost-effective than any alternative available today.

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