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February 06, 2016 9:00 PM ET

Healthcare Equipment and Supplies

Company Overview of Eckert & Ziegler Radiopharma Gmbh

Company Overview

Eckert & Ziegler Radiopharma Gmbh manufactures imaging products used for diagnosis and treatment of cancer. The company develops molecular imaging equipment. Eckert & Ziegler Radiopharma Gmbh was formerly known as Eckert & Ziegler Medizintechnik GmbH. The company was founded in 2005 and is based in Berlin, Germany. The company operates as a subsidiary of Eckert & Ziegler Strahlen & Medizintechnik AG.

Robert-Rössle-Straße 10

Berlin,  13125


Founded in 2005


49 30 94 10 84 280


49 30 94 10 84 470

Key Executives for Eckert & Ziegler Radiopharma Gmbh

Eckert & Ziegler Radiopharma Gmbh does not have any Key Executives recorded.

Eckert & Ziegler Radiopharma Gmbh Key Developments

Eckert & Ziegler Radiopharma Gmbh Receives Recommendation from the European Medicines Agency for Approval of Pharmaceutical (68) Ge/(68) Ga Generators

Eckert & Ziegler Radiopharma GmbH has received a recommendation from the European Medicines Agency for approval of its pharmaceutical (68) Ge/(68) Ga generators. This achievement marks the conclusion of a comprehensive decentralized evaluation procedure and the first time a gallium generator has been approved for the clinical development of highly specific diagnostic agents. Approval for sale in the respective countries is expected within the next one to two months. Gallium generators provide an inexpensive alternative for radiolabeling diagnostic probes using positron emission tomography (PET), an imaging process that can be used to determine whether tissue is diseased. The process is mainly used in cancer treatment. Until now, fluorine-18 or carbon-11 PET radioisotopes have usually been used to radiolabel diagnostic probes; these radioisotopes are produced using cyclotrons that are capitally intensive, large-scale dedicated installations requiring millions in investment. In contrast, the gallium generator is approximately the size of a thermos and can be sourced for far less money, lowering costs and increasing flexibility at nuclear medicine clinics. Once it has received approval, Eckert & Ziegler will also submit its documents to the U.S. Food and Drug Administration (FDA), establishing a Drug Master File with the agency. This will allow parties interested in developing new drugs to refer to the dossier and use the generator in clinical tests of medications and in other settings.

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