AfriSummit
AfriSummit brings together stakeholders from the pharmaceutical industry and medical device sector, regulatory bodies, and leading solution providers from across Africa and globally. It aims to drive the unity of healthcare regulations, enhancing access to safe, effective, and high-quality medicines. Key topics will include convergence in Regulations, compliance, and innovative pathways. The summit will also offer specialized workshops on Pharmacovigilance and eCTD, equipping attendees with the latest advancements and best practices in the field. AfriSummit comprises several sub-events, including PharmaReg, MedDevReg, Pharmacovigilance, and eCTD Training.
Location
Grand Nile Tower
16 Nile Corniche
Cairo
Egypt
+971 4 299 9398
Grand Nile Tower
16 Nile Corniche
Cairo
Egypt
+971 4 299 9398
Highlights ⭐
- PharmaReg AfriSummit: Designed for pharmaceutical professionals dedicated to advancing regulatory affairs across Africa, its mission is to foster robust partnerships between regulatory authorities and the industry, streamline application and approval processes, and expedite the introduction of new medications for a healthier Africa.
- MedDevReg AfriSummit: The summit aims to unite National Regulatory Affairs Agencies and Industry stakeholders to navigate the intricacies of Medical Device and IVD Regulations, and facilitate market access across Africa. Over two days, it offers a collaborative platform for manufacturers and distributors to explore avenues for introducing life-changing devices into the African market.
- Pharmacovigilance AfriSummit: Designed exclusively for seasoned pharmacovigilance professionals, this intensive training equips you with the tools and knowledge to optimize your daily practice. By delving into regulatory intricacies and real-world implications, you'll emerge primed to navigate the evolving landscape of medication safety with confidence.
- eCTD Training: Enhance your knowledge of electronic Common Technical Document (eCTD) at AfriSummit's specialized training. Dive into the intricacies of eCTD submission formats, regulatory requirements, and best practices. Gain practical skills to navigate the electronic submission process effectively, ensuring compliance and efficiency in pharmaceutical regulatory affairs.
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Last update:
October 6, 2024
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