Consultants Day

Due to unforeseen circumstances, our Open House event at the New Brighton Lab has been postponed; please check back soon for the new date and further details.

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This will be a full day event starting at 9AM - 5PM. 

We invite you to join us in New Brighton for an enriching Consultants Day, specifically designed to enhance your expertise in the MedTech sector. This event promises to be filled with discussions about innovation, knowledge, and networking, providing a deep dive into the complexities and advancements in medical technology. Prepare to engage in thought-provoking discussions, connect with industry peers, and enjoy a selection of fine catering that complements our day of learning and collaboration.

Please register by Friday April 26, 2024.

Important note: Participation is free of charge. The number of participants is limited, and we can accept a maximum of two registrations per company. Therefore, it is best to register today.

Roundtable Topics:

1. "Product Testing: Mastering Product Evaluation"

This session is for consultants looking to deepen their understanding of MedTech product testing. We’ll explore advanced testing methodologies, regulatory insights, and quality assurance strategies essential for ensuring the highest standards in MedTech products.

2. "Application Acumen: Simplifying Complex Processes"

Dive into the intricacies of the MedTech application process. This roundtable will provide you with the knowledge to guide your clients through efficient application strategies, addressing both local and international compliance issues.

3. "Audit Essentials: Ensuring Client Readiness"

Enhance your advisory skills with insights into the latest audit practices in the MedTech field. This discussion will guide you on how to prepare your clients for audits, in order to support them in maintaining compliance and operational efficiency. 

4. "Clinical Data Insights: Maximizing Data Utilization"

Discover how to effectively utilize clinical data for legacy and new medical devices. This session is crucial for consultants seeking to advise their clients on compiling and leveraging clinical evidence to support MedTech innovations.

5. "Global Compliance: Navigating MDSAP Challenges"

Get up to speed with the Medical Device Single Audit Program’s latest developments and requirements. This roundtable is essential for consultants advising clients on international market strategies and compliance.

6. "IVD Innovations: Adapting to Changing Timelines"

Explore the dynamic world of In-Vitro Diagnostics, focusing on managing the EU Commission proposal to extend the timelines for compliance. This topic is key for consultants advising clients on staying ahead in this specialized and rapidly evolving sector.

7. "AI & Cybersecurity in MedTech"

This session offers an intensive overview of integrating AI and fortifying cybersecurity in MedTech. It covers AI applications, cybersecurity strategies, and regulatory compliance, empowering consultants to guide MedTech innovation with security and efficiency.