We are pleased to announce that as of July 2010, the Danish Medicines Agency has granted Biomonitor A/S a GLP-authorization.
For further information please contact:
Arsalan Kharazmi, CEO, Biomonitor A/S.
E-mail: ak @ biomon.dk, Phone: +45 39179797
Archive for July, 2010Biomonitor A/S achieves GLP-authorizationJuly 7th, 2010We are pleased to announce that as of July 2010, the Danish Medicines Agency has granted Biomonitor A/S a GLP-authorization. For further information please contact: Biomonitor is proud to present the first IVD cell-based assay kits for NAb detection iLiteTM anti-human IFN-beta-1a - used for the detection of Neutralizing antibodies against IFN-beta-1a and iLiteTM anti-human IFN-beta-1b - used for the detection of Neutralizing antibodies against IFN-beta-1b Prolonged therapies with many biopharmaceuticals, including IFN-alpha and IFN-beta, often lead to development of neutralizing antibodies (NAb). The development of these NAbs is a problem which if not recognized may jeopardize therapeutic efficacy of the IFN treatment and cause side effects from local and/or circulating immune complexes. Treatment with the above mentioned IFN biopharmaceuticals is costly. Monitoring patients for antibody development is therefore both rational and cost-effective.
Biomonitor A/S achieves GMO classificationJuly 7th, 2010We are pleased to announce that as of June 2010, the laboratories of Biomonitor A/S have been classified for working with genetically modified organisms (GMO). For further information please contact: Biomonitor A/S completes Round C private placementJuly 7th, 2010We are pleased to announce that as of March 2010, Biomonitor A/S has completed Round C private placement with the Danish venture capital company Sunstone Capital A/S. For further information please contact: |