2-Day Seminar: Biological Evaluation of Medical Devices (London, United Kingdom - October 2-3, 2019) - ResearchAndMarkets.com
DUBLIN--(BUSINESS WIRE)--Feb 22, 2019--The “Biological Evaluation of Medical Devices” conference has been added to ResearchAndMarkets.com’s offering.
Key guidance on how to use the ISO 10993 series of standards and successfully apply a risk management approach to the biological evaluation of medical devices.
New for 2019
The ISO 10993 series of standards covering biological evaluation of medical devices is well established and regulatory authorities worldwide expect compliance. In Europe compliance with the standards will be the easiest way to meet the relevant essential product safety requirements of the Medical Device Regulation. Understanding a risk management approach to biological evaluation is essential.
This seminar will provide key guidance on how to use the standards and successfully apply a risk management approach to the biological evaluation of medical devices. There will be plenty of time for interactive discussion with experts in this field.
Who Should Attend?
This seminar will be of importance to those in the medical device industry from the following departments:
Programme Day One
General principles of biological risk management
Interactive session: Hazardous situations
Reviewing existing data
Interactive session: Evaluating chemical data
Programme Day Two
Quantitative toxicological risk assessment (QTRA)
Interactive session: Gap analysis
Risk assessment and control
Interactive session: Risk reduction
Interactive session: Risk review
Q & A discussion
Summary and conclusions
For more information about this conference visit https://www.researchandmarkets.com/research/tbxbh2/2day_seminar?w=4
View source version on businesswire.com:https://www.businesswire.com/news/home/20190222005305/en/
Laura Wood, Senior Press Manager
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Related Topics:Medical Devices
INDUSTRY KEYWORD: HEALTH MEDICAL DEVICES
SOURCE: Research and Markets
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PUB: 02/22/2019 09:44 AM/DISC: 02/22/2019 09:44 AM