Resources

1 min read

December Image of the Month

YOU BE THE PATHOLOGIST!

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3 min read

Amending Regulation for MDR / IVDR: Key Takeaways for the Diagnostics Industry

Yesterday, the EU Parliament adopted the regulation amending EU 2017/745 (MDR) and EU 2017/746 (IVDR) aiming to protect patients by ensuring the...

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Person Responsible for Regulatory Compliance (PRRC) – EU & Swiss Regulations

This training currently has no open sessions. If you would like to attend, please leave us a message, and we will inform you when a new date is...

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August Image of the Month

YOU BE THE ANATOMIST!

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1 min read

Substance-based Device Regulation

This training currently has no open sessions. If you would like to attend, please leave us a message, and we will inform you when a new date is...

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1 min read

November Image of the Month

You be the Imaging Specialist Which state-of-the-art technology provides detailed images like this one and enables you to tailor your vascular...

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5 min read

Artificial Intelligence (AI), General Data Protection Regulation (GDPR) and Cybersecurity: 10 Misconceptions About Medical Device Software

Medical Device Software (MDSW) is a growing, fast-evolving industry. However, manufacturers must often face a regulatory framework which does not...

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4 min read

Built to Fit Your Needs: Our CDMO Capabilities

Learn about our capabilities and offerings as a CDMO We sat down with Bill Croisetiere (VP, Integrated Supply Chain), Chris Vigneau (VP,...

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2 min read

Prioritizing Patient Safety and Fostering Innovation with the MHRAs New Roadmap for Medical Devices

On January 9, the United Kingdom (UK)’s Medicines and Healthcare Products Regulatory Agency (MHRA) released a regulatory framework – Roadmap towards...

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Digital Experiences for the Sandwich Generation

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