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X-ORIGINAL-URL:https://www.sahpra.org.za
X-WR-CALDESC:Events for SAHPRA
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TZID:Africa/Johannesburg
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TZOFFSETFROM:+0200
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DTSTART:20220101T000000
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BEGIN:VEVENT
DTSTART;TZID=Africa/Johannesburg:20231106T180000
DTEND;TZID=Africa/Johannesburg:20231106T193000
DTSTAMP:20260501T105034
CREATED:20231106T162207Z
LAST-MODIFIED:20260209T131036Z
UID:15237-1699293600-1699299000@www.sahpra.org.za
SUMMARY:Webinar | Importance of Reporting Adverse Events to SAHPRA | #MedSafetyWeek
DESCRIPTION:The South African Health Products Regulatory Authority (SAHPRA) is commemorating the #MedSafetyWeek2023 campaign\, in collaboration with South African Pharmacy Council (SAPC)\, by hosting a webinar focused on the Importance of Reporting Adverse Events. \nThe #MedSafetyWeek is an international social media campaign organised every year by the Uppsala Monitoring Centre (UMC) to raise awareness of adverse events and national reporting systems. \nYou have an opportunity to learn and engage with SAHPRA and SAPC colleagues on key safety and reporting issues. \nWhat you will learn about: \n\nReporting side effects\nSide effects experienced at health facilities\nRole of pharmacies and patient safety\n\nDate: 06 November 2023\nTime: 18:00 \n\nPresentations:\nJHB Health District\nExpanded Program On Immunisation In South Africa \n  \nWebinar recording:
URL:https://www.sahpra.org.za/event/webinar-importance-of-reporting-adverse-events-to-sahpra-medsafetyweek/
LOCATION:Virtual
CATEGORIES:Webinar
ATTACH;FMTTYPE=image/jpeg:https://www.sahpra.org.za/wp-content/uploads/2023/11/mailer-banner-Importance-of-Reporting-Adverse-Events-to-SAHPRA.jpg
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BEGIN:VEVENT
DTSTART;TZID=Africa/Johannesburg:20231114T090000
DTEND;TZID=Africa/Johannesburg:20231116T180000
DTSTAMP:20260501T105034
CREATED:20231113T094948Z
LAST-MODIFIED:20231113T180835Z
UID:15275-1699952400-1700157600@www.sahpra.org.za
SUMMARY:Good Regulatory Practices and Technical Competencies
DESCRIPTION:This workshop will provide an exchange of information and capacity building between the South African Health Products Regulatory Authority\, SAPHRA and partner reference NRAs including the WHO\, USFDA\, TGA\, HSA\, ANVISA\, covering the core international references for medical device regulatory. The workshop objective is to support and advance to strengthen the soft infrastructure of medical device regulatory framework to incorporate global lessons learned from the COVID-19 pandemic\, to better prepare for future health emergencies\, to prevent the implementation of unnecessary regulatory barriers to medical technologies\, to improve general MD NRA public administration and general public health. \n  \nDate: 14 November 2023\nTime: 9:00 – 17:30 Pretoria\, South Africa (2:00 am – 10:30 ET)\nPlatform: Hybrid (In-person: Southern Sun Pretoria Hotel\, Cnr. Steve Biko and\, Pretorius St\, Arcadia\, Pretoria\, 0083). Please register here for virtual or in-person participation. \n\nRegister for hybrid event here.
URL:https://www.sahpra.org.za/event/good-regulatory-practices-and-technical-competencies/
LOCATION:Hybrid [Venue: Innovation Hub]
CATEGORIES:Hybrid meeting
ATTACH;FMTTYPE=image/jpeg:https://www.sahpra.org.za/wp-content/uploads/2023/11/event-banner.jpeg
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