2013-02-14 15:01:42 - This online event with theme "Risk-based Software Validation for Quality System software and Medical Device Data Systems" featured by ComplianceOnline will be conducted February 26th, 2013.

This 90-minute webinar on software validation will provide the information required to establish a system for validating software under FDA’s Quality System Regulation/cGMP. This includes validating any software used for manufacturing and testing of medical devices. In addition it will cover the approaches to validating Medical Device Data Systems software.

Learning Objectives:

- Developing or updating your software validation system to one based on risk
- Complying with FDA requirements for manufacturing, testing and quality software
- Complying with FDA requirements for validation of software in MDDS products
- Methods of creating software requirements documents
- Principles for creating a software risk analysis
- Elements required in a software validation study

Who will Benefit:

This medical

device software validation webinar will provide valuable assistance to the following personnel:
- Quality management personnel
- Regulatory affairs personnel
- Quality engineers
- Design engineers for MDDS products
- Validation engineers
- Quality auditors

Get more info and register online for the Risk-based Software Validation for Quality System software and Medical Device Data Systems (MDDS) at conferix.com/risk-based-software-validation-for-quality-system-s ..

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