2 Day Virtual Biological Evaluation of Medical Devices Training Course: Ensure Compliance with the ISO 10993 Series of Standards for the Biological Evaluation of Medical Devices (Jan 21st-22nd, 2026)

Dublin, Nov. 03, 2025 (GLOBE NEWSWIRE) -- The "Biological Evaluation of Medical Devices Training Course (Jan 21st - Jan 22nd, 2026)" training has been added to ResearchAndMarkets.com's offering.

Ensure compliance with the ISO 10993 series of standards for the biological evaluation of medical devices, as it is well-established and expected by regulatory authorities worldwide.

In the European Union, compliance with these standards is crucial for meeting the essential safety requirements outlined in the Medical Device Regulation (MDR). Understanding and implementing a comprehensive risk management strategy for biological safety is therefore paramount.

This seminar offers essential guidance on effectively utilising the ISO 10993 standards and integrating a robust risk management approach into the biological evaluation process of medical devices. Participants will have ample opportunity to engage in interactive discussions with industry experts, gaining practical insights and best practices.

Attendees will emerge equipped with the knowledge and tools necessary to navigate regulatory requirements, mitigate risks, and ensure the safety and efficacy of medical devices in compliance with global standards.

Benefits of attending

Understand biological risk managementClarify the requirements of ISO 10993-1Learn what endpoints need to be addressed in a biological risk assessmentEstablish how much chemical characterisation is necessaryExplore the FDA's approach to ISO 10993Comprehend the Medical Device Directive (MDD) safety requirements vs the Medical Device Regulation (MDR) safety requirementsRecognise how extractables and leachables impact medical device safetyDiscuss the Japanese and Chinese requirements

Certifications:

CPD: 12 hours for your recordsCertificate of completion

Who Should Attend:

Regulatory affairsR&DProduct safety/toxicologyAnalytical chemistryRisk assessment and risk managementMaterials research and evaluation

It will also be of interest to regulatory authorities, Notified Bodies and CROs supporting the medical device industry.

For more information about this training visit https://www.researchandmarkets.com/r/udji3f

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