Mecomed and the Regulatory Affairs Professionals Society (RAPS) have come together for the first time to produce the 2025 MEA MedTech Regulatory Summit, convening 30 January 2025 at the voco Dubai in Dubai, UAE. This one-day, interactive summit unites leaders from regulatory agencies, industry, and other key stakeholder groups for focused discussion and exchange on the most-pressing issues and challenges impacting the region.
“The Middle East and Africa encompass a growing and diverse MedTech hub in the regulatory community, with rapidly expanding new business opportunities,” said Rami Rajab, Chief Executive Officer, Mecomed. “As companies look to expand their global footprint, there is a heightened need for education, professional development and meaningful connections to support growth—and the advancement of patient care. Now more than ever, navigating the complex web of international regulations becomes a strategic imperative and accelerating the implementation of Regulatory reliance in practice is key.”
Designed specifically for senior decision makers and regulators across the medical device community, the 2025 MEA MedTech Regulatory Summit will ensure that regulatory professionals are able to stay up-to-date and navigate complexities during an era of rapid change. Topics to be explored include the changing regulatory landscape in the Middle East, Africa, Europe and North America, as well as the impact of AI and software on the regulatory landscape and regulatory operations. Additionally, attendees will experience health authority updates and participate in discussions on evolving global regulatory strategies and planning.
The programme for this summit is carefully curated by experts across the MedTech community to ensure the highest quality discussions, knowledge exchange, and collaboration opportunities. Planning committee members include:
- Dr. Bassil Akra, Founder/Executive Consultant, AKRA TEAM
- Carol Attieh, Growth Emerging Markets (GEM) Regulatory Lead, Boston Scientific Middle East FZ LLC
- Rana Chalhoub, Regulatory Affairs Director, Mecomed
- Nataliya Deych, Vice President Regulatory Affairs EMEA, LATAM, Canada, Edwards Life Sciences
- Brian Savoie, Senior Vice President, Education & International Programs, Regulatory Affairs Professionals Society (RAPS)
- Peter Schroeer, Vice President Regulatory Affairs EMEA and Canada, Johnson & Johnson
- Graeme Tunbridge, Senior Vice President Global Regulatory and Quality, Medical Devices, BSI
Registration is open for the 2025 MEA MedTech Regulatory Summit, and the complete programme agenda and speaker lineup will be announced in the coming weeks. To learn more, visit www.meamedtech.org.
