Iso 13485 2016 Medical Devices A Practical Guide: An essential resource for medical device professionals and stakeholders, this guide provides a comprehensive overview of the Iso 13485 2016 standard. It covers key requirements, good practices and implementation guidance across all stages of a product’s life cycle – from design to production, distribution and post-market surveillance. Comprehensive and easy to read, it is an invaluable resource for those seeking to ensure their products are compliant with industry standards.