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Webinar e Formazione Online

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Presidi Medico Chirurgici: come il regime transitorio si traduce in Italia

The new EU-GMP Annex 1: New features and Eurofins consultancy support

Viral safety – An overview of regulatory landscape and testing strategy

Virucidal testing: test methods overview for regulatory purposes and claim support - Current situation and future perspectives

Challenges in virus clearance studies design and execution for tissue-based medical devices

ISO 10993-18:2020, a practical approach to competent authorities expectations

Pharmaceutical impurities: Regulatory updates and challenges from a toxicologist point of view

EU importers – requirements from manufacturers

EU MDR: State of play and challenges to compliance

BPR, principles and regulatory overview

New approach methodologies (NAMs) for medical devices

Challenges in virus clearance studies design and execution for tissue-based medical devices to be submitted to US FDA

Information requirements for biocidal product authorisation: Part 1

How to design pre-clinical combined studies evaluating both long term systemic toxicity and local tissue effects

ISO TC 194 latest updates

Information requirements for biocidal product authorisation part 2: human health and environmental risk assessments

Etichettatura Ambientale

On site courses: Techniques for usability testing

Cleaning validation: statistica applicata al monitoraggio

ISO 10993-17:2023, what’s new

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