Ilona Putz joins the Editorial Advisory Board of the Journal of Medical Device Regulation
The Journal of Medical Device Regulation (JMDR) is pleased to announce the appointment of Ilona Putz to its Editorial Advisory Board.
A highly experienced healthcare executive and founder of PULONA Emerging Markets FZE, Ilona brings nearly four decades of experience across the pharmaceutical and medical device sectors, with particular expertise in market access, regulatory affairs and emerging markets in the Middle East and North Africa (MENA).
Since founding PULONA Emerging Markets in the United Arab Emirates in 2008, Ilona has focused on helping healthcare companies understand and navigate market access and regulatory frameworks across the MENA region. Her career has included senior commercial and regulatory positions with multinational companies including MSD, GlaxoSmithKline Beecham and HEXAL. As Regional Head for the Middle East at Sandoz International, she was responsible for driving commercial growth and market entry strategies across the region.
“We are delighted to welcome Ilona Putz to the Editorial Advisory Board of the JMDR,” said Editorial Director Victoria Clark. “Her extensive experience in medical device and pharmaceutical regulation, combined with her deep knowledge of the MENA region and emerging markets, will bring valuable perspective to the JMDR and its international readership”.
Ilona is also an established speaker and contributor to industry literature. Since 2006, she has regularly presented on pharmaceutical and medical device regulatory affairs in the MENA region and has spoken at international industry events. She has also authored detailed analyses of medical device regulations in various countries.
Ilona’s appointment further strengthens the JMDR’s international editorial network and its commitment to providing medical device professionals with practical, authoritative and globally relevant regulatory intelligence.
About the Journal of Medical Device Regulation
The Journal of Medical Device Regulation (JMDR), published by Global Regulatory Press, provides regulatory intelligence and analysis for professionals working in the global medical device industry. Through expert articles, in-depth analyses, regulatory news and podcasts, the JMDR helps manufacturers, regulatory affairs professionals and other industry stakeholders understand regulatory developments and their implications for market access and compliance.
For more information on the Journal of Medical Device Regulation, please contact Marija Capek
(tel: +44 7916 443811; email: sales@globalregulatorypress.com) or visit GlobalRegulatoryPress.com.
