Regulatory Consulting

Home News Regulatory Consulting

Navigating Dual Certification: How to Stay Compliant Across the UK and EU

28 Jan

Navigating Dual Certification: How to Stay Compliant Across the UK and EU

As we enter 2026, the post-Brexit regulatory landscape for medical devices continues to evolve, presenting both challenges and opportunities for manufacturers targeting the UK (Great Britain) and EU markets.

Stay Compliant with EN ISO 10993-1:2025 Updates

The publication of EN ISO 10993-1:2025 represents a key milestone for all medical device manufacturers who will be required, during 2026, to assess the need to update their biological evaluation documentation. Maytal can support you in a comprehensive and structured manner to address this regulatory update efficiently and without slowing down your ongoing projects

We use cookies

This website uses cookies in order to enhance the overall user experience.

Customize

Cookie essenziali

Ci sono alcuni cookie che dobbiamo includere affinché determinate pagine web funzionino. Per questo motivo, non richiedono il tuo consenso.

maytaleu_cookie_consent

1 year 1 month 1 day

Utilizzato per memorizzare le preferenze di consenso ai cookie dell'utente.
maytaleu_session

2 hours

Utilizzato per identificare la sessione di navigazione dell'utente.
XSRF-TOKEN

2 hours

Utilizzato per proteggere sia l'utente che il nostro sito web dagli attacchi di tipo cross-site request forgery.

More details

Follow Us

Regulatory Consulting

Navigating Dual Certification: How to Stay Compliant Across the UK and EU

Stay Compliant with EN ISO 10993-1:2025 Updates

Categories

Follow Us

Regulatory Consulting

Navigating Dual Certification: How to Stay Compliant Across the UK and EU

Stay Compliant with EN ISO 10993-1:2025 Updates

Categories

Tags