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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:20220101T000000
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DTSTART;TZID=Europe/Moscow:20230201T090000
DTEND;TZID=Europe/Moscow:20230201T163000
DTSTAMP:20260425T071157
CREATED:20221129T100728Z
LAST-MODIFIED:20221129T100728Z
UID:5591-1675242000-1675269000@bawazirpharma.com
SUMMARY:Health and Herbal Products Development Process and Regulatory Approval 1 February 2023 Riyadh
DESCRIPTION:Note:  All training programs require physical presence and will be held in Riyadh at Bawazir Pharma Center\n\n\n\nFEES\nSAUDI RIYAL\n\n\nREGISTRATION FEES \n\nSAR 1500.00\n\n\n\nEARLY BIRDS REGISTRATION FEE  \nPAY YOUR FEE BEFORE 31 January 2023.\n\nSAR 1000.00\n\n\n\n\nOVERVIEW\nUnderstanding drug regulatory affairs in the GCC region is  very important for persons working in pharmaceutical  sector in the region. This course is specifically designed for  persons working in the regulatory affairs departments or  related fields\, who need knowledge of the SFDA and GCC  regulatory processes. This training will also enhance  understanding and be beneficial to persons who work in  clinical research\, data management\, basic research\,  project management and marketing\, etc. \n  \nDownload Brochure Health and Herbal Products Development Process\, and Regulatory Approval 1 February 2023\, Riyadh\n  \nLEARNING OBJECTIVES \nAt the conclusion of this training\, participants will be able to: \n\nDefine the key principles and processes used by the Saudi Food and Drug Authority (SFDA) in regulatory submission and approval.\nDefine official regulatory policies and other issues pertinent to a successful SFDA and GCC regulatory strategy\nDescribe the requirements for marketing applications for\n\nherbal and health products and document preparation. \n\nRecognize SFDA oversight and processes during the post- approval phase.\nInteract appropriately with the SFDA during all phases of drug registration\n\n  \nKEY TOPICS \n\nPrincipals of Regulatory Affairs (RA) and Legal Framework\nPrinciples of Products licensing and Evaluation\nData requirements for health and herbal products\nOverview of the SFDA Electronic systems\n\n  \nWHO WILL ATTEND \nProfessionals working in: \n\nPharma Regulatory Affairs\nFresh Graduate\nScientific Office Managers\nRegulatory Authorities.\nDossier Management\nPharmacist\nCompliance
URL:https://bawazirpharma.com/event/health-and-herbal-products-development-process-and-regulatory-approval-1-february-2023-riyadh/
LOCATION:Bawazir Pharma Office\, PJW5+79\, Riyadh\, 13513\, Saudi Arabia
ORGANIZER;CN="Bawazir Pharma Consulting":MAILTO:info@bawazirpharma.com
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