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Bringing a medical device to market is not a straight path from innovation to approval. It’s shaped by shifting global frameworks, compressed timelines and exacting regulatory demands. For most companies, this creates familiar tension; internal teams drive for speed while regulators urge caution. In that push-and-pull, progress is often at risk. That’s where Sobel Consultancy comes in—not just as a regulatory expert, but as a true strategic partner, helping companies stay focused, aligned and on course when the stakes are highest. Clients turn to Sobel for direction that helps them know when to press ahead, when to pause and how to make those decisions in line with the bigger business pict... Read more
For dental professionals looking to thrive in a competitive industry, effective marketing isn’t just an advantage—it’s essential. Yet, many dental professionals don’t fully understand the power of traditional or digital marketing, causing them to miss valuable opportunities to attract new patients and enhance their practice. On the flip side, some practices have tried marketing before, only to be disappointed by partnerships that overpromised and underdelivered, le... Read more
Sandra Marcela Cortés Gómez, Chief Nursing Officer, Fundacion Santa Fe de Bogotá – Colombia
Claudio Soto Angelo, Chief Medical Officer, Clínica Los Coihues
Roberto Caldeira Cury, Vice President of Customer Service and Experience Units, Dasa
Dino Scanio, MPH, Doctoral Candidate, Multiservice Hospital Director of Clinics, Driscoll Children’s Hospital
Dan Mather, MSN, RN, Director of Clinic Operations, Salina Regional Health Center
Anthony Piotrkowski, Director of Regulatory Affairs, STERIS
Amos Chery, Director, Pharmacy Operations and Regulatory Compliance, MedStar Health
The Future of Medical Device Regulation
Reflecting this trend, Latin America’s medical device regulatory affairs market is projected to reach approximately $446.2 million by 2030, growing at a CAGR of 9.4 percent from 2025 to 2030.
A slew of technological trends is driving the industry forward. Regulatory intelligence platforms automate the monitoring of regional policy updates, helping consultants stay ahead of changes and ensure clients remain compliant in real time. Cloud-based document management systems streamline the submission and tracking of regulatory dossiers, reducing delays and improving stakeholder transparency. AI-driven data analytics enhance risk assessments and market entry strategies by providing predictive insights based on historical approvals and regional trends.
This edition of Healthcare Business Review Latin America spotlights the region’s leading medical device regulatory consultants who are setting a new standard for what it means to be regulatory-ready in Latin America. It features insights from Dr. Amos Chery, director of pharmacy operations and regulatory compliance at MedStar Health, who discusses how pharmacy operations must balance innovation with compliance. He emphasizes the role of training, technology and proactive strategies to navigate automation, outsourcing and evolving regulations in healthcare. Roberto Caldeira Cury, executive medical director at Dasa, discusses how the organization is transforming healthcare in Latin America by embracing precision medicine and data-driven diagnostics.
The magazine also features Sobel Consultancy, a strategic regulatory partner known for turning complex compliance demands into clear, actionable strategies. Through scalable infrastructure and expert guidance, it helps medical device companies align fast-paced innovation with evolving global regulations.
We hope this edition helps your organization build the partnerships it needs to sharpen its competitive edge in the medical regulatory space.