Knowledge: Managing RFIs for Clinical Trial Applications in CTIS
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Product information: Nordic Contract Pharma Organisation
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Product information: Overview of Arex Advisor’s service offer
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Press release: Regulatory Affairs Expert Anna Ravnefjord joins Arex Advisor
Stockholm, Sweden Arex Advisor AB are pleased to announce that Anna Ravnefjord joins the company as Regulatory Affairs Expert. Anna brings a wealth of experience in global Regulatory Affairs, with a particular focus on clinical development. Her proficiency extends to strategy work in several development phases, as well as complex regulatory environments in pharma and […]