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Resources

Explore our extensive resources to uncover more about RCA's expertise in life sciences consulting.

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Webinars

Supplier Quality Management Risks

Ensuring a successful product launch of a connected device requires that your supply chain be capable and available thru the different design and development stages. However, supplier quality management issues...
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Webinars

Common Submission Pitfalls and Best Practices

This presentation will explore the critical challenges of data integrity and accessibility within the context of AI-powered, FDA-regulated medical devices. It will delve into the importance of robust and reliable...
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Webinars

ÃÛ¶¹ÊÓÆµ Data Integrity and Accessibility Concerns

This presentation will explore the critical challenges of data integrity and accessibility within the context of AI-powered, FDA-regulated medical devices. It will delve into the importance of robust and reliable...
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Webinars

ÃÛ¶¹ÊÓÆµ Requirements & Software Development for ÃÛ¶¹ÊÓÆµ Cybersecurity

This on-demand webinar explores the evolving cybersecurity requirements for medical devices under the U.S. FDA’s CDRH and the EU’s MDR and IVDR frameworks. It provides a detailed overview of the...
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Webinars

Connected Devices and Quality Management: Meeting ÃÛ¶¹ÊÓÆµ Demands Under cGMP and EUMDR

Does your Quality Management System have the right capabilities to ensure that your XBU Connect Device will be safe and effective? Placing a connected device in the marketplace presents new...
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Webinars

510(k) Marketing Submissions and Predetermined Change Control Plans

This presentation will explore the intersection of Artificial Intelligence (AI) in medical devices and the FDA’s 510(k) premarket notification process. It will highlight and address the challenges posed by the...
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