Switzerlabnd's Biopartners GmbH says that it will request a re-assessment from the European Medicines Agency (EMEA) in support of its novel interferon beta-1a product Biferonex, after receiving a negative opinion from the Agency's Committee on Medicinal Products for Human Use (CHMP).
According to EMEA procedures, Biopartners will continue its work to accomplish the registration of Biferonex. The re-examination will last approximately three to four months, the firm noted.
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