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Approval of LifePearl® Microspheres as a Class III device in Europehttps://www.terumo-europe.com/en-emea/news/approval-of-lifepearl®-microspheres-as-a-class-iii-device-in-europeApproval of LifePearl® Microspheres as a Class III device in EuropeLeuven, Belgium18/01/2018 23:00:00<p>Terumo Europe N.V, announces the approval of LifePearl Microspheres as a Class III device in Europe.  This approval also expands the loadable chemotherapeutic drugs to include Idarubicin and Epirubicin.</p>
Terumo Provides Update on Impact from Hurricane Mariahttps://www.terumo-europe.com/en-emea/news/terumo-provides-update-on-impact-from-hurricane-mariaTerumo Provides Update on Impact from Hurricane MariaTokyo, Japan12/10/2017 22:00:00
Terumo welcomes the positive reimbursement decision for QuiremSpheres® in Belgium as of 1 October 2017https://www.terumo-europe.com/en-emea/news/terumo-welcomes-the-positive-reimbursement-decision-for-quiremspheres®-in-belgium-as-of-1-october-2017Terumo welcomes the positive reimbursement decision for QuiremSpheres® in Belgium as of 1 October 2017Leuven, Belgium20/09/2017 22:00:00<p style="text-align:justify;">Terumo welcomes an important milestone for QuiremSpheres® in Belgium and in Europe. The decision to add QuiremSpheres® to the list of reimbursed radiopharmaceutical products in Belgium was published in the Belgian Official Gazette on 20 September 2017. This will allow hospitals wishing to use QuiremSpheres® to treat patients with advanced unresectable liver cancer to be reimbursed as of 1 October 2017.</p>
Terumo Launches QuiremSpheres® Microspheres in Europehttps://www.terumo-europe.com/en-emea/news/terumo-launches-quiremspheres®-microspheres-in-europeTerumo Launches QuiremSpheres® Microspheres in EuropeTokyo, Japan18/09/2017 22:00:00<p><font size="3">Terumo Corporation (TSE: 4543)announced today thatit has launched QuiremSpheres® microspheres on September 18 in Europe. QuiremSpheres®are available in Europe with plans for expansion in areas outside of Europe in the future.</font></p><font size="3"></font>
Terumo Announces European Medicines Agency Validates Marketing Authorization Application for a Biosimilar to Be Formulatedhttps://www.terumo-europe.com/en-emea/news/terumo-announces-european-medicines-agency-validates-marketing-authorization-application-for-a-biosimilar-to-be-formulatedTerumo Announces European Medicines Agency Validates Marketing Authorization Application for a Biosimilar to Be FormulatedTokyo, Japan22/05/2017 22:00:00<p>​<span>To Accelerate Global Expansion of PLAJEX™</span></p>