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X-WR-CALNAME:Prof. Bawazir Pharma Consulting Center
X-ORIGINAL-URL:https://bawazirpharma.com
X-WR-CALDESC:Events for Prof. Bawazir Pharma Consulting Center
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DTSTART:20200101T000000
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DTSTART;TZID=Europe/Moscow:20210315T090000
DTEND;TZID=Europe/Moscow:20210315T173000
DTSTAMP:20260425T133128
CREATED:20210126T123447Z
LAST-MODIFIED:20210323T142006Z
UID:3884-1615798800-1615829400@bawazirpharma.com
SUMMARY:Post Approval Activities and Compliance: Variations Guideline 15 March\, 2021 Riyadh
DESCRIPTION:  \n\n\n\nFEES\nSAUDI RIYAL\n\n\nREGISTRATION FEES \nSAR 1500.00\n\n\nEARLY BIRDS REGISTRATION FEE  \nPAY YOUR FEE BEFORE 10 March 2021.\nSAR 1000.00\n\n\n\nOVERVIEW \nThis course will provide an overview and analysis of the various regulatory activities that take place post-approval: In particular\, the current regulatory climate will be discussed in depth and numerous examples will be provided to illustrate effective filing of notification techniques. Common issues which have caused difficulties for pharmaceutical firms will also be discussed.  The training will discuss in detail the GCC guideline for variations management and post approval commitment. \n  \nLEARNING OBJECTIVES \n\nDescribe the role of regulatory affairs on meeting SFDA regulations\nUnderstand the regulatory activities that take place post approval of their products.\nDiscuss the post approval commitment that must be met.\nUnderstand the post approval commitment and how to help company comply with them\n\n  \nKEY TOPICS \n\nPost-approval commitments\nPV\nPSUR\nRMMs\nVariations management\n\nWHO WILL ATTEND \nProfessionals working in: \n\nRegulatory Affair staff\nScientific office staff\nProduction manager\nQA Manger\nQC Manager
URL:https://bawazirpharma.com/event/post-approval-activities-and-compliance-variations-guideline-15-march-2021-riyadh/
LOCATION:Bawazir Pharma Office\, PJW5+79\, Riyadh\, 13513\, Saudi Arabia
ORGANIZER;CN="Bawazir Pharma Consulting":MAILTO:info@bawazirpharma.com
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