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Tilburg Area, Netherlands Netherlands

Senior Regulatory Affairs Scientist at Qdossier/eCTDconsultancy

Medical / Health Care / Pharmaceuticals

Visionary concerning regulatory information management, considering the right-first-time creation of information and documentation (content) and the ability to see the scientific content in context of use. Content concerns regulatory-, chemical/pharmaceutical-, nonclinical- and clinical information justifying the consistently produced high quality drugs with a favourable benefit-risk ratio for a clearly defined patient population when used in accordance with the prescribing information.