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Webinars & Seminars

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A special thank you to all 8700+ registrants of our 2024 webinars.


Thank you for your participation, we are more than happy to have you in our upcoming webinars.

Upcoming Webinars/Seminars

Nanomatériaux dans les dispositifs médicaux

Reprocessing of Reusable Medical Devices

Ready to tackle FDA registration

Keep calm and be ready for new ISO 10993-1

Viral Clearance of Medical Devices

Usability & ergonomic requirements for MD

Past Webinars/Seminars

PFAS Medical Device Regulations

Biological Evaluation Plans

Sterilization Validations

SDLC Key Points & Cybersecurity for FDA

What is a "good" BEP?

Alternative Methods for Medical Devices

New ISO 18562 Series

Implementation of ISO 13485

Nanomaterials in Medical Devices

The Dynamic Duos

Sterilisation validations, EO vs Irradiation

Medical Device Package Testing

Reprocessing Challenges & Considerations

No repetition of animal testing

Bioburden determination on Medical Devices

Usability techniques for compliance

Special Hemocompatibility Testing

Questions from Notified Bodies

Clean and safe – the pure validation strategy

Pyrogens, alternative methods

Medical Device Pyrogenicity

CE/MDR versus FDA submission

The post market surveillance

Ophthalmic delivery systems

Strategic Implementation of ISO 10993-17

Stability studies of medical devices

E&L study for drug-like medical devices

Handling Cytotoxicity Failure: not the end

Navigating through the jungle of ISO 11607

New Approach of Toxicological Risk assessment

Selecting correct deterministic CCIT method

ISO 10993-17:2023, what’s new

ISO TC 194 latest updates

Pre-clinical combined studies

New approach methodologies (NAMs)

MDR: challenges to compliance

EU importers, requirements from manufacturers

ISO 10993-18:2020, A Practical Approach

Hemocompatibility Testing

Virus Clearance Studies (US FDA)

Virus Clearance Studies (EU)

S(p)oiler Alarm - Reusable Medical Devices

Breathing gas pathway devices

Reprocessing of Reusable Medical Devices

In-vitro testing/regulatory compliance

MDR submission

Ethylene Oxide

Navigating the Full Biocompatibility Workflow

Principles for Validation of Reprocessing

Biocompatibility Testing
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