Writing Software Specifications for Medical Devices
Abstract:In this article, Dev Raheja, a renowned expert on Medical Devices, their software and regulatory requirements, discusses how to write effective software for medical devices, the risks, requirements and specifications.
Compliance Trainings
Design History File (DHF), Device Master Record (DMR) and DHR Utilizing the Principles of Lean Documents and Lean Configuration
By - Jose Mora
On Demand Access Anytime
By - Jose Mora
On Demand Access Anytime
QA Agreements for ISO 13485:2019 and other Regulatory Compliance
By - Betty Lane
On Demand Access Anytime
By - Betty Lane
On Demand Access Anytime
Compliance Standards
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