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E-BooksWriting In–House Medical Device Software in Compliance with EU, UK, and US Regulations



Writing In–House Medical Device Software in Compliance with EU, UK, and US Regulations
Free Download Writing In-House Medical Device Software in Compliance with EU, UK, and US Regulations
English | 2024 | ISBN: 1032293500 | 291 Pages | PDF (True) | 4 MB
This book is a comprehensive guide to producing medical software for routine clinical use. It is a practical guidebook for medical professionals developing software to ensure compliance with medical device regulations for software products intended to be sold commercially, shared with healthcare colleagues in other hospitals, or simply used in-house.



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