Dieser Basiskurs gibt Ihnen einen Einblick in regulatorische Anforderungen und Prozesse zur erfolgreichen Entwicklung von Medizinprodukten und In-vitro Diagnostika. Welche Elemente müssen Entwicklungsprojekte enthalten, damit Zeit- und Kostenrahmen eingehalten werden und die regulatorischen Anforderungen von Anfang an berücksichtigt werden?
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Up to date in der Pharmakovigilanz (PV) - Was Zulassungsinhaber in der EU wissen sollten?
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In the competitive healthcare industry, effectively engaging both patients and healthcare professionals is critical for…
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