Events

See Amra Racic, VP of Government Strategy at Veeva MedTech, present alongside Joshua Silverstein, Regulatory Science and Policy Director at Philips on global regulatory trends and what's on the horizon for 2025.

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Join Veeva MedTech at the largest gathering of Medical Affairs Professionals as we fully realize our place as a strategic pillar in the biopharmaceutical and MedTech industries. Register

Registration for Veeva MedTech Summit 2025 in Austin is open. Summit is two days of networking and 40+ educational sessions covering topics across clinical, quality, regulatory, commercial, technology, and medical affairs. Register

Join Veeva MedTech at the largest gathering of Medical Affairs Professionals in EU as we fully realize our place as a strategic pillar in the biopharmaceutical and medtech industries. Register

Join Veeva MedTech at RAPS Euro Convergence, the most comprehensive regulatory affairs conference in Europe, focusing on the latest topics and developments in healthcare products in Europe and beyond — with sessions in medical devices, IVDs, pharmaceuticals, combination products, regulatory business, AI, software, and cybersecurity. Register

The MedTech Forum is the largest health and medical technology industry conference in Europe. Join Veeva MedTech and other industry leaders, leading innovators, and investors to discuss the future opportunities in the medical technology sector. Learn More

Join Veeva MedTech at The European Medical Device Summit, a leading medtech event in Düsseldorf, offering actionable strategies to advance medical device development, design, product development technologies, and regulatory affairs. Learn More

Join Veeva MedTech and the world’s top medtech executives at the leading medical technology event. Learn More

Join Veeva MedTech at RAPS Convergence, the largest and most well-recognized annual gathering of regulatory professionals and innovators. Learn More

Registration for Veeva MedTech Summit 2025 in Madrid is open. Summit is two days of networking and 40+ educational sessions covering topics across clinical, quality, regulatory, commercial, technology, and medical affairs. Register

Jennifer Kerr, President at Cook Research, shares insight on how Cook Research is leveraging digital platforms to unify clinical operations and speed study execution, including:

Industry trends to improve clinical study performance

Factors that accelerate implementation

Achieving visibility, oversight, and collaboration

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B.Braun & Integra describe the future of patient care, how to reach a more diverse audience, and how to design patient-centric trials. Access Now

Becki Brasher, Medtronic, and Bassil Akra shares insights and best practices for managing claims, commercial content, and compliance, including:

Advertising regulations and risks

Ownership, substantiation, approval, and field compliance monitorization

Do’s and don'ts for a solid claims foundation

Accelerating speed to market and competitive advantage

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Medical Affairs is evolving and enabling fast, compliant, strategic engagement with HCPs and KOLs. Connectivity across channels is imperative to get products to patients and to understand their needs.

Join this webinar for insights on:

-Medical Affairs trends and challenges

-How top medtechs are adapting processes, roles, and approaches

-Driving efficiency and value across the organization leveraging technology

-Unifying scientific exchange, content, and intelligence with Veeva Medical Suite

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Join this webinar to learn how B.Braun modernized clinical management to speed trials and support global growth. You'll discover how their approach to modernizing trial management leverages cloud technology through phased implementation, robust digital frameworks, global process harmonization, and continuous change management to ensure success. Access Here

Ascensia Diabetes Care, Global Program Lead, Ntianu Onumonu will share how the company implemented a claims and content management program that reduces review and approval times, enhances compliance, and streamlines marketing operations.

Ntianu will share:

1. How to navigate organizational complexities
2. Critical steps of implementation and adoption How automation is reducing time in the review process
3. Practical advice to gradually improve claims and content with tangible results

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João Martins, Associate Director of Regulatory Affairs Strategy at Abbott, and Megha Deviprasad Iyer, Director of Global Strategic Regulatory Affairs at Thermo Fisher Scientific will address the growing challenges for regulatory affairs professionals amid increasing global health regulations and shifting priorities.

They will discuss:

1. Scaling resources to stay ahead of complex medtech regulations
2. Addressing the impact of evolving regulations on internal workflow and compliance strategies
3. Driving innovation and expediting product market entry

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