Roser Ibern Oriol

Regulatory expert in interdisciplinary teams; team leader in Global Regulatory Affairs. Planning, organization and coordination of regulatory activities with affiliates and partners (Europe, Central and South America, CEE, Middle East and Australia), within Global Regulatory Affairs as well as with different departments in Headquarters, including preparation of registration documents (administrative, quality, clinical, preclinical) Experience with scientific advice (EMA, national)

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Experience in European Procedures (MRP as CMS) and National procedures in Germany

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- Experience in European procedures (MRP and DCP as RMS), national procedures in Europe, South America, Africa and Asia; coordination of regulatory activities with partners; preparation of registration documents (administrative, quality, clinical, preclinical). - Experience with innovative and generic medicinal products.

- Experience in European Procedures (MRP as CMS, CP), National procedures in Spain for both human and veterinary medicinal products; relationship with headquarters in Germany. - Experience with innovative and OTC medicinal products.