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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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BEGIN:VTIMEZONE
TZID:Europe/Moscow
BEGIN:STANDARD
TZOFFSETFROM:+0300
TZOFFSETTO:+0300
TZNAME:MSK
DTSTART:20240101T000000
END:STANDARD
END:VTIMEZONE
BEGIN:VEVENT
DTSTART;TZID=Europe/Moscow:20250707T090000
DTEND;TZID=Europe/Moscow:20250708T163000
DTSTAMP:20260425T150725
CREATED:20250404T000650Z
LAST-MODIFIED:20250617T184541Z
UID:7019-1751878800-1751992200@bawazirpharma.com
SUMMARY:Comprehensive SFDA Pharmacovigilance System Explained Basic and Intermediate 7-8 July 2025 Riyadh Saudi Arabia
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 6500.00\n\n\nEARLY BIRDS REGISTRATION FEE  \nPAY YOUR FEE BEFORE 5 July 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_7-8 July_2025 Riyadh\, Saudi Arabia\n  \nLEARNING OBJECTIVES \nAt the conclusion of this training\, participants will be able to: \n\nDefine the key principles and processes of pharmacovigilance\n\n\nDefine official regulatory policies and other issues pertinent to SFDA Pharmacovigilance System\nDescribe the component of the PV System\nUnderstand the role and responsibilities of the QPPV\nUnderstand national pharmacovigilance sub-system file (national PSSF)\nRecognize SFDA oversight and processes during the post-approval phase.\nUnderstand ADR case assessment\, PSUR and risk management.\nInteract appropriately with the SFDA regarding PV\nUnderstand the process of PV inspection and audits.\n\nKEY TOPICS \n\nIntroduction to Pharmacoepidemiology and Pharmacovigilance\nPharmacovigilance systems and their quality systems\nPharmacovigilance System Master File\nQualified Person Responsible for Pharmacovigilance in Saudi Arabia\nRisk Management Systems\nManagement and Reporting of Adverse Reactions to Medicinal Products\nPeriodic Safety Update Reports\nPost-Authorization Safety Studies\nSignal Management\nSafety Communication\nRisk Minimization Measures\nPharmacovigilance Inspections\nPharmacovigilance Audits\nBasic concepts of vaccines and adverse events following immunization\n\nWHO WILL ATTEND \nProfessionals working in: \n\nQPPV\nPharma Regulatory Affairs\nCountry Managers\nScientific Office Managers\nContract Research Organizations (CROs)\nRegulatory Authorities.\nPharmacist\nCompliance
URL:https://bawazirpharma.com/event/comprehensive-sfda-pharmacovigilance-system-explained-basic-and-intermediate-7-8-july-2025-riyadh-saudi-arabia/
LOCATION:Bawazir Pharma Office\, PJW5+79\, Riyadh\, 13513\, Saudi Arabia
ORGANIZER;CN="Bawazir Pharma Consulting":MAILTO:info@bawazirpharma.com
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Moscow:20250806T090000
DTEND;TZID=Europe/Moscow:20250806T160000
DTSTAMP:20260425T150725
CREATED:20250727T210547Z
LAST-MODIFIED:20250727T211428Z
UID:7168-1754470800-1754496000@bawazirpharma.com
SUMMARY:Basics of Drug Regulatory Affairs SFDA System Explained Training 6 August 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  5  August 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. \nDownload Brochure Basics of Drug Regulatory Affairs SFDA Explained 6 August 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-6-august-2025-riyadh/
LOCATION:Bawazir Pharma Office\, PJW5+79\, Riyadh\, 13513\, Saudi Arabia
ORGANIZER;CN="Bawazir Pharma Consulting":MAILTO:info@bawazirpharma.com
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Moscow:20250811T090000
DTEND;TZID=Europe/Moscow:20250812T160000
DTSTAMP:20260425T150725
CREATED:20250730T195708Z
LAST-MODIFIED:20250730T195708Z
UID:7186-1754902800-1755014400@bawazirpharma.com
SUMMARY:Comprehensive SFDA Pharmacovigilance System Explained Basic and Intermediate 11-12 August 2025 Riyadh Saudi Arabia
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 6500.00\n\n\nEARLY BIRDS REGISTRATION FEE  \nPAY YOUR FEE BEFORE 9 August 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_11-12 August_2025 Riyadh\, Saudi Arabia\n  \nLEARNING OBJECTIVES \nAt the conclusion of this training\, participants will be able to: \n\nDefine the key principles and processes of pharmacovigilance\n\n\nDefine official regulatory policies and other issues pertinent to SFDA Pharmacovigilance System\nDescribe the component of the PV System\nUnderstand the role and responsibilities of the QPPV\nUnderstand national pharmacovigilance sub-system file (national PSSF)\nRecognize SFDA oversight and processes during the post-approval phase.\nUnderstand ADR case assessment\, PSUR and risk management.\nInteract appropriately with the SFDA regarding PV\nUnderstand the process of PV inspection and audits.\n\nKEY TOPICS \n\nIntroduction to Pharmacoepidemiology and Pharmacovigilance\nPharmacovigilance systems and their quality systems\nPharmacovigilance System Master File\nQualified Person Responsible for Pharmacovigilance in Saudi Arabia\nRisk Management Systems\nManagement and Reporting of Adverse Reactions to Medicinal Products\nPeriodic Safety Update Reports\nPost-Authorization Safety Studies\nSignal Management\nSafety Communication\nRisk Minimization Measures\nPharmacovigilance Inspections\nPharmacovigilance Audits\nBasic concepts of vaccines and adverse events following immunization\n\nWHO WILL ATTEND \nProfessionals working in: \n\nQPPV\nPharma Regulatory Affairs\nCountry Managers\nScientific Office Managers\nContract Research Organizations (CROs)\nRegulatory Authorities.\nPharmacist\nCompliance
URL:https://bawazirpharma.com/event/comprehensive-sfda-pharmacovigilance-system-explained-basic-and-intermediate-11-12-august-2025-riyadh-saudi-arabia/
LOCATION:Bawazir Pharma Office\, PJW5+79\, Riyadh\, 13513\, Saudi Arabia
ORGANIZER;CN="Bawazir Pharma Consulting":MAILTO:info@bawazirpharma.com
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Moscow:20250908T090000
DTEND;TZID=Europe/Moscow:20250909T163000
DTSTAMP:20260425T150725
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
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Moscow:20250915T090000
DTEND;TZID=Europe/Moscow:20250915T160000
DTSTAMP:20260425T150725
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
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Moscow:20251103T090000
DTEND;TZID=Europe/Moscow:20251103T160000
DTSTAMP:20260425T150725
CREATED:20250811T161402Z
LAST-MODIFIED:20251029T224204Z
UID:7445-1762160400-1762185600@bawazirpharma.com
SUMMARY:Basics of Drug Regulatory Affairs SFDA System Explained
DESCRIPTION:Date of training 3 November 2025 Riyadh Saudi Arabia \n\n\n\nFEES\nSAUDI RIYAL\n\n\nREGISTRATION FEES \nSAR 3400.00\n\n\nEARLY BIRD REGISTRATION FEE  \nPAY YOUR FEE BEFORE  1  November 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. \nDownload Brochure Basics of Drug Regulatory Affairs SFDA Explained 3 November 2025 Riyadh
URL:https://bawazirpharma.com/event/basics-of-drug-regulatory-affairs-sfda-system-explained/
LOCATION:Bawazir Pharma Office\, PJW5+79\, Riyadh\, 13513\, Saudi Arabia
ORGANIZER;CN="Bawazir Pharma Consulting":MAILTO:info@bawazirpharma.com
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Moscow:20251125T090000
DTEND;TZID=Europe/Moscow:20251126T160000
DTSTAMP:20260425T150725
CREATED:20251011T152102Z
LAST-MODIFIED:20251221T223620Z
UID:7438-1764061200-1764172800@bawazirpharma.com
SUMMARY:Comprehensive SFDA Pharmacovigilance System Explained Basic and Intermediate
DESCRIPTION:Date of training 25-26 November 2025 Riyadh Saudi Arabia\n\n\n\nFEES\nSAUDI RIYAL\n\n\nREGISTRATION FEES \nSAR 6500.00\n\n\nEARLY BIRDS REGISTRATION FEE  \nPAY YOUR FEE BEFORE 24 November 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_25-26 November 2025 Riyadh
URL:https://bawazirpharma.com/event/comprehensive-sfda-pharmacovigilance-system-explained-basic-and-intermediate/
LOCATION:Bawazir Pharma Office\, PJW5+79\, Riyadh\, 13513\, Saudi Arabia
ORGANIZER;CN="Bawazir Pharma Consulting":MAILTO:info@bawazirpharma.com
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Moscow:20260119T090000
DTEND;TZID=Europe/Moscow:20260119T160000
DTSTAMP:20260425T150725
CREATED:20251221T225829Z
LAST-MODIFIED:20260117T075234Z
UID:7574-1768813200-1768838400@bawazirpharma.com
SUMMARY:Basics of Drug Regulatory Affairs SFDA System Explained
DESCRIPTION:Date of training 19 January 2026 Riyadh Saudi Arabia \n\n\n\nFEES\nSAUDI RIYAL\n\n\nREGISTRATION FEES \nSAR 3400.00\n\n\nEARLY BIRD REGISTRATION FEE  \nPAY YOUR FEE BEFORE  18  January 2026.\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. \nDownload Brochure Basics of Drug Regulatory Affairs SFDA Explained 19 January 2026 Riyadh
URL:https://bawazirpharma.com/event/basics-of-drug-regulatory-affairs-sfda-system-explained-2/
LOCATION:Bawazir Pharma Office\, PJW5+79\, Riyadh\, 13513\, Saudi Arabia
ORGANIZER;CN="Bawazir Pharma Consulting":MAILTO:info@bawazirpharma.com
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Moscow:20260120T090000
DTEND;TZID=Europe/Moscow:20260121T160000
DTSTAMP:20260425T150725
CREATED:20251221T222603Z
LAST-MODIFIED:20260117T074941Z
UID:7565-1768899600-1769011200@bawazirpharma.com
SUMMARY:Comprehensive SFDA Pharmacovigilance System Explained Basic and Intermediate
DESCRIPTION:Date of training 20-21 Januaruy 2026 Riyadh Saudi Arabia\n\n\n\nFEES\nSAUDI RIYAL\n\n\nREGISTRATION FEES \nSAR 6500.00\n\n\nEARLY BIRDS REGISTRATION FEE  \nPAY YOUR FEE BEFORE 18 Januaruy 2025.\n\nSAR 5200.00\n\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_20-21 January_2026 Riyadh
URL:https://bawazirpharma.com/event/comprehensive-sfda-pharmacovigilance-system-explained-basic-and-intermediate-2/
LOCATION:Bawazir Pharma Office\, PJW5+79\, Riyadh\, 13513\, Saudi Arabia
ORGANIZER;CN="Bawazir Pharma Consulting":MAILTO:info@bawazirpharma.com
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Moscow:20260406T090000
DTEND;TZID=Europe/Moscow:20260406T160000
DTSTAMP:20260425T150725
CREATED:20260226T122937Z
LAST-MODIFIED:20260226T123551Z
UID:7614-1775466000-1775491200@bawazirpharma.com
SUMMARY:Basics of Drug Regulatory Affairs SFDA System Explained
DESCRIPTION:Date of training 6 April 2026 Riyadh Saudi Arabia \n\n\n\nFEES\nSAUDI RIYAL\n\n\nREGISTRATION FEES \nSAR 3400.00\n\n\nEARLY BIRD REGISTRATION FEE  \nPAY YOUR FEE BEFORE  3  April 2026.\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. \nDownload Brochure Basics of Drug Regulatory Affairs SFDA Explained 6 April 2026 Riyadh
URL:https://bawazirpharma.com/event/basics-of-drug-regulatory-affairs-sfda-system-explained-3/
LOCATION:Bawazir Pharma Office\, PJW5+79\, Riyadh\, 13513\, Saudi Arabia
ORGANIZER;CN="Bawazir Pharma Consulting":MAILTO:info@bawazirpharma.com
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Moscow:20260407T090000
DTEND;TZID=Europe/Moscow:20260408T160000
DTSTAMP:20260425T150725
CREATED:20260226T125441Z
LAST-MODIFIED:20260226T125441Z
UID:7620-1775552400-1775664000@bawazirpharma.com
SUMMARY:Comprehensive SFDA Pharmacovigilance System Explained Basic and Intermediate
DESCRIPTION:Date of training 7-8 April 2026 Riyadh Saudi Arabia\n\n\n\nFEES\nSAUDI RIYAL\n\n\nREGISTRATION FEES \nSAR 6500.00\n\n\nEARLY BIRDS REGISTRATION FEE  \nPAY YOUR FEE BEFORE 3 April 2026.\n\nSAR 5200.00\n\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_7-8 April_2026 Riyadh
URL:https://bawazirpharma.com/event/comprehensive-sfda-pharmacovigilance-system-explained-basic-and-intermediate-3/
LOCATION:Bawazir Pharma Office\, PJW5+79\, Riyadh\, 13513\, Saudi Arabia
ORGANIZER;CN="Bawazir Pharma Consulting":MAILTO:info@bawazirpharma.com
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Moscow:20260409T090000
DTEND;TZID=Europe/Moscow:20260409T160000
DTSTAMP:20260425T150725
CREATED:20260321T013612Z
LAST-MODIFIED:20260330T192700Z
UID:7633-1775725200-1775750400@bawazirpharma.com
SUMMARY:Common Technical Documents (CTD) and (eCTD) preparation
DESCRIPTION:Date of training 9 April 2026 Riyadh Saudi Arabia \n\n\n\nFEES\nSAUDI RIYAL\n\n\nREGISTRATION FEES \nSAR 2900.00\n\n\nEARLY BIRDS REGISTRATION FEE  \nPAY YOUR FEE BEFORE 7 April 2026. \n\nSAR 2000.00\n\n\n\n\nOVERVIEW \nThis course will offer insight into the compilation of the  eCTDs\, share experience and best practices gained during eCTD  submissions in the GCC\, explain the eCTD review and lifecycle process and the upcoming eCTD requirements. \n  \nDownload Brochure Common Technical Documents (CTD) and (eCTD) preparation 9_April_2026 Riyadh
URL:https://bawazirpharma.com/event/common-technical-documents-ctd-and-ectd-preparation/
LOCATION:Bawazir Pharma Office\, PJW5+79\, Riyadh\, 13513\, Saudi Arabia
ORGANIZER;CN="Bawazir Pharma Consulting":MAILTO:info@bawazirpharma.com
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Moscow:20260511T090000
DTEND;TZID=Europe/Moscow:20260511T160000
DTSTAMP:20260425T150725
CREATED:20260419T140602Z
LAST-MODIFIED:20260419T140937Z
UID:7663-1778490000-1778515200@bawazirpharma.com
SUMMARY:Basics of Drug Regulatory Affairs SFDA System Explained
DESCRIPTION:Date of training 11 May 2026 Riyadh Saudi Arabia \n\n\n\nFEES\nSAUDI RIYAL\n\n\nREGISTRATION FEES \nSAR 3400.00\n\n\nEARLY BIRD REGISTRATION FEE  \nPAY YOUR FEE BEFORE  9  MAY 2026.\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. \nDownload Brochure Basics of Drug Regulatory Affairs SFDA Explained 11 May 2026 Riyadh
URL:https://bawazirpharma.com/event/basics-of-drug-regulatory-affairs-sfda-system-explained-4/
LOCATION:Bawazir Pharma Office\, PJW5+79\, Riyadh\, 13513\, Saudi Arabia
ORGANIZER;CN="Bawazir Pharma Consulting":MAILTO:info@bawazirpharma.com
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Moscow:20260512T090000
DTEND;TZID=Europe/Moscow:20260513T160000
DTSTAMP:20260425T150725
CREATED:20260419T143503Z
LAST-MODIFIED:20260420T090935Z
UID:7671-1778576400-1778688000@bawazirpharma.com
SUMMARY:Comprehensive SFDA Pharmacovigilance System Explained Basic and Intermediate
DESCRIPTION:Date of training 12-13 May 2026 Riyadh Saudi Arabia\n\n\n\nFEES\nSAUDI RIYAL\n\n\nREGISTRATION FEES \nSAR 6500.00\n\n\nEARLY BIRDS REGISTRATION FEE  \nPAY YOUR FEE BEFORE 11 May 2026.\n\nSAR 5200.00\n\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_12-13 May_2026 Riyadh
URL:https://bawazirpharma.com/event/comprehensive-sfda-pharmacovigilance-system-explained-basic-and-intermediate-4/
LOCATION:Bawazir Pharma Office\, PJW5+79\, Riyadh\, 13513\, Saudi Arabia
ORGANIZER;CN="Bawazir Pharma Consulting":MAILTO:info@bawazirpharma.com
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