Introduction

This webinar will discuss regulatory requirements for the medical device software development process and how the documentation needed for MDD technical files and for FDA submission can be developed as part of that process.

Useful links

• Further event details More information about the event

Sponsorship & supporting organisations

ComplianceOnline

Venue

Online Event

Online Event, 2600 E. Bayshore Road, California, Palo Alto, 94303, United States

Contact information

Mr Referral
2600 E. Bayshore Road, Palo Alto, 94303, United States of America
+1-650-620-3915
Contact us by email

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