ComplianceOnline

IEC 62304 – Medical Device Software Life Cycle Process Standard – Overview and Summary of Requirements for Software Development

  • By: Staff Editor
  • Date: September 22, 2011
Webinar All Access Pass Subscription Abstract:

The IEC 62304 is a global harmonized standard adopted by the US and EU. It gives life cycle requirements for medical device software as well as medical software.

This article gives an overview of the standard and a summary of the IEC 62304 requirements for software development.

Bookmark and Share

Trending Compliance Trainings

Challenges of an Effective Change Control Program
By - Kenneth Christie
On Demand Access Anytime
Implementation and Management of GMP Data Integrity
By - Danielle DeLucy
On Demand Access Anytime
FDA Compliance and Clinical Trial Computer System Validation
By - Carolyn Troiano
On Demand Access Anytime
Biocompatibility Testing; what you need to know
By - Mike Colvin
On Demand Access Anytime
Best Sellers
You Recently Viewed
    Loading