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X-ORIGINAL-URL:https://bawazirpharma.com
X-WR-CALDESC:Events for Prof. Bawazir Pharma Consulting Center
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TZID:Europe/Moscow
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BEGIN:VEVENT
DTSTART;TZID=Europe/Moscow:20250908T090000
DTEND;TZID=Europe/Moscow:20250909T163000
DTSTAMP:20260425T065438
CREATED:20250824T110733Z
LAST-MODIFIED:20251010T211232Z
UID:7224-1757322000-1757435400@bawazirpharma.com
SUMMARY:Comprehensive SFDA Pharmacovigilance System Explained Basic and Intermediate 8-9 September 2025 Riyadh Saudi Arabia
DESCRIPTION:  \n\n\n\nFEES\nSAUDI RIYAL\n\n\nREGISTRATION FEES \nSAR 6500.00\n\n\nEARLY BIRDS REGISTRATION FEE  \nPAY YOUR FEE BEFORE 6 September 2025.\nSAR 5200.00\n\n\n\nOVERVIEW \nUnderstanding Pharmacovigilance System in Saudi Arabia is very important for persons working in pharmaceutical sector in the region. This course is specifically designed for persons working as Qualified Person of Pharmacovigilance (QPPV) in the regulatory affairs departments or related fields\, who need knowledge of the SFDA Pharmacovigilance System and processes. This training will also enhance understanding and be beneficial to persons who work in clinical research\, data management\, basic research\, and marketing\, etc. \n  \nDownload Brochure Comprehensive SFDA Pharmacovigilance System Explained Basic and Intermediate_8-9 September_2025 Riyadh\n 
URL:https://bawazirpharma.com/event/comprehensive-sfda-pharmacovigilance-system-explained-basic-and-intermediate-8-9-september-2025-riyadh-saudi-arabia/
LOCATION:Bawazir Pharma Office\, PJW5+79\, Riyadh\, 13513\, Saudi Arabia
ORGANIZER;CN="Bawazir Pharma Consulting":MAILTO:info@bawazirpharma.com
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BEGIN:VEVENT
DTSTART;TZID=Europe/Moscow:20250915T090000
DTEND;TZID=Europe/Moscow:20250915T160000
DTSTAMP:20260425T065438
CREATED:20250824T112915Z
LAST-MODIFIED:20250824T112915Z
UID:7235-1757926800-1757952000@bawazirpharma.com
SUMMARY:Basics of Drug Regulatory Affairs SFDA System Explained Training 15 September 2025 Riyadh
DESCRIPTION:Note:  This training program requires physical presence and will be held in Riyadh at Bawazir Pharma Center \n\n\n\nFEES\nSAUDI RIYAL\n\n\nREGISTRATION FEES \nSAR 3400.00\n\n\nEARLY BIRD REGISTRATION FEE  \nPAY YOUR FEE BEFORE  12  September 2025.\n\nSAR 2400.00\n\n\n\n\nOVERVIEW \nUnderstanding drug regulatory affairs 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 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 Basics of Drug Regulatory Affairs SFDA Explained 15 September 2025 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 regulatory strategy.\nDescribe key differences between National and the Gulf Cooperation Council Drug Registration regulatory requirements.\nDescribe the requirements for marketing applications for drugs and biologics\, New Drug Application (NDA)\, Biosimilares\, Generic drugs\, herbal and health products and document preparation.\nRecognize SFDA oversight and processes during the post-approval phase.\nInteract appropriately with the SFDA during all phases of drug registration\nUnderstand the regulatory requirements for prescription drug labelling and advertising/promotion.\n\n  \nKEY TOPICS \n\nPrincipals of Regulatory Affairs (RA) and Legal Framework\nSFDA overview and pharmaceutical institutions licensing\nPrinciples of Products licensing and Evaluation\nGMP Inspection and Products Pricing\nOverview of the pharmacovigilance system\nPrinciples of Products Classifications and Listing\nProducts Import\, Release and Advertising\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/basics-of-drug-regulatory-affairs-sfda-system-explained-training-15-september-2025-riyadh/
LOCATION:Bawazir Pharma Office\, PJW5+79\, Riyadh\, 13513\, Saudi Arabia
ORGANIZER;CN="Bawazir Pharma Consulting":MAILTO:info@bawazirpharma.com
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