Events

Best Practices for Transforming Quality and Regulatory with Technology

The medtech industry is facing a more complex regulatory landscape than ever before. With EU MDR maintenance and IVDR preparation alongside growing pressures from competition and rising costs of manufacturing, many are exploring new ways to improve their bottom lines.

To ensure ongoing compliance, patient safety, business longevity, and competitive advantage, medtech companies should embrace digital transformation, which allows organizations to support cross-functional data efficiency, increase 24/7 insights, reduce compliance challenges, and speed time to market. However, the selection and adoption of digital technologies require focus and thorough analysis.

In this webinar, we highlight:

• Successful approaches to digital transformation
• The role of technology in shifting from reactive to proactive approach
• What to look for in a digital solution to support sustainable compliance globally

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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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Learn how Alcon, Baxter, and Roche Diagnostics are transforming their regulatory operations models to remain agile and effective through the ever-changing global regulatory landscape, including:

Challenges and opportunities of our current environment

Ensuring commercial continuity with global regulatory collaboration and transparency

Addressing the "New Normal" regulatory model with a technology-based program

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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

Veeva MedTech Summit 2023 took place in Chicago, but you can visit the event page for agenda and recorded highlights. View Content

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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Veeva MedTech Summit, Europe on 5-7 November will bring together medtech professionals and experts to hear the latest news and market trends, experience innovative technology, network, and share best practices. View Content

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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