{"id":5306,"date":"2021-02-04T16:08:00","date_gmt":"2021-02-04T15:08:00","guid":{"rendered":"https:\/\/q-finity.de\/auditierung-der-gvp-prozesse-und-der-darunterliegenden-computergestuetzten-systeme-bei-einem-pharmahersteller\/"},"modified":"2026-07-07T14:47:34","modified_gmt":"2026-07-07T12:47:34","slug":"auditing-of-the-gvp-processes-and-the-underlying-computer-aided-systems-at-a-pharmaceutical-manufacturer","status":"publish","type":"post","link":"https:\/\/q-finity.de\/en\/auditing-of-the-gvp-processes-and-the-underlying-computer-aided-systems-at-a-pharmaceutical-manufacturer\/","title":{"rendered":"Auditing of the GVP processes and the underlying computer-aided systems at a pharmaceutical manufacturer"},"content":{"rendered":"<p>A pharmaceutical manufacturer hires QFINITY&infin; to conduct a routine audit of the pharmacovigilance system to verify compliance with regulatory requirements. The audit also includes the relevant computerized systems that influence processes in the pharmacovigilance area, as well as the special role of a qualified person in the company.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>A pharmaceutical manufacturer hires QFINITY\u221e to conduct a routine audit of the pharmacovigilance system to verify compliance with regulatory requirements. 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