Medical Device

Best Practices for Medical Device Development

March 14, 2016

Medical device developers must take into account numerous safety, quality and risk factors to ensure the durability and safety of their devices. Developers must also adhere to strict risk management processes and life cycle requirements that may vary regionally. Our friends at Seapine Software have generated the whitepaper below to help developers navigate this shifting terrain and understand the best practices for exposing risk throughout the product development life cycle.

Exposing Risk Throughout Your Product Development Lifecycle

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Best Practices for Medical Device Development

Generis Generis is a Full-Service Organizer of World Class Business Summits.

Women in Leadership with Birgit Fuchs, VP, Supply Chain, Automotive at Infineon [Speaker Spotlight]

Resilience and Innovation in Manufacturing: Evonik's Journey to Supply Chain Excellence with Thomas Schamberg, Ph.D., SVP of Supply Chain Excellence at Evonik Industries [Speaker Spotlight]

Empowering Transformation with Change Management Solutions in Manufacturing with Adel Emam, Chief Operating Officer, MENA at JBS Foods [Speaker Spotlight]

Best Practices for Medical Device Development

Generis Generis is a Full-Service Organizer of World Class Business Summits.

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