Training

At Medifocs we firmly believe that the development of professional skills of an individual and a company should be based on an effective and continuous training and updating process.

Which is why we organise tailored training courses for the medical device industry, including:

Risk Management for Medical Devices and ISO 14971:2019
Quality Management System and ISO 13485:2016
Design control and Product Development Management
Regulation (EU) 2017/745
Post-Market Surveillance under Regulation (EU) 2017/745

All courses include interactive effectiveness checks, specific assessments of each trainee and an attendance certificate.

Choose Medifocs to Improve your company’s skills!

Write to us to arrange a training course tailored to your needs.

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Guidance on appropriate surveillance regarding the transitional provisions under Article 120 of the MDR with regard to devices covered by certificates according to the MDD or the AIMDD. MDCG 2022-4

Bozza dell’atto di implementazione relativo a specifiche comuni per i dispositivi medici senza destinazione d’uso medica elencati nell’Allegato XVI del Regolamento (UE) 2017/745

Training

Write to us to arrange a training course tailored to your needs.

Subscribe to our newsletter to receive updates on the world of pharmaceuticals and medical devices.

Guidance on appropriate surveillance regarding the transitional provisions under Article 120 of the MDR with regard to devices covered by certificates according to the MDD or the AIMDD. MDCG 2022-4

Bozza dell’atto di implementazione relativo a specifiche comuni per i dispositivi medici senza destinazione d’uso medica elencati nell’Allegato XVI del Regolamento (UE) 2017/745

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