Risk Management during device design according to ISO14971 - Webinar By GlobalCompliancePanel

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In the medical device development process, it has become a regulatory necessity to implement an effective risk management plan to fulfill the requirements of ISO14971. Manufacturers, however, still struggle to comply with ISO14971 and find a meaningful way to introduce risk management to the overall operating framework. Additionally, the presentation provides practical tips to comply with ISO14971, implement risk management, and minimize the administrative burdens imposed to handle the additional process.

Areas Covered in the Session
Basic principles of risk management

Risk management planning and procedures

Hazard and risk analysis

Documentation of risk management activities

Practical tips for implementing risk management processes

Who Will Benefit:
Project Managers

System Engineers

Regulatory Affairs

Compliance Managers

Regulatory and Compliance Associates


Price List:
Live : $245.00
Corporate live : $995.00
Recorded : $295.00

webinars@globalcompliancepanel.com
http://www.globalcompliancepanel.com

Phone: 800-447-9407
Fax: 302-288-6884