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Webinar on Test Methods and Standards for Design Verification & Validation

Event Details

Webinar on Test Methods and Standards for Design Verification & Validation

Time: July 29, 2016 from 1pm to 2pm
Location: Online
Street: 5939 Candlebrook Ct
City/Town: Mississauga
Website or Map: https://compliancetrainings.c…
Phone: 4169154458
Event Type: webinar
Organized By: Compliance Trainings
Latest Activity: Jul 4, 2016

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Event Description

Description :

Design Control is an integral part of any quality system in regulated industries. FDA Quality System regulation, Quality System Inspection Techniques (QSR and QSIT) and ISO 13485: 2016 have specific product verification and validation requirements that must be fulfilled in the medical device industry. FDA is getting more and more stringent about product design requirements for risk management and to fulfill its mandate for safety and efficacy of all medical devices.

The design controls are now being expected from outside equipment manufacturers (OEM) and all suppliers to the medical device industry. This webinar will educate you on the key areas that you need to focus on to fulfill the design control and testing requirements for your medical device at various phases of your product development.

Areas Covered in the Session :

Product development process overview

Applicable design verification and validation requirements

Testing requirements including the pertinent ISO Standards

Translation of user requirements into design inputs

Role of testing and regulatory requirements

Focusing on critical to customer and quality requirements

Design verification and design validation activity cycles

Traceability and risk management at all stages

Design outputs and documentation in DMR (Device Master Records) and DHR (Device History Records)

Proof for how design outputs meet functional and operational requirements

Compatibility of the design with components and other accessories

Test requirements to fulfill acceptance criteria for final products

How to withstand regulatory scrutiny

How are changes and their effects controlled and documented during the device life cycle?

Summary

Who Will Benefit:

Senior management

Middle management

Research & Development

Quality Engineers and Auditors

Manufacturing Engineers

Regulatory Affairs Professionals

Quality Assurance & Quality Control Personnel

Device Design Team

Device Development Team

Device Manufacturing Team

Verification and/or Validation planning, execution and documentation for devices.

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