Netzealous LLC DBA - Compliance4All, Online
2017-11-08
Overview: The US FDA expects that as part of a product development Design Control
Program risk management will be conducted. FDA recommends using ISO
14971 as a guide and has accepted it as a recognized standard.
Why should you Attend: FDA expects that as part of a product development program risk management
will be conducted. FDA recommends using ISO 14971 as a guide and has
accepted it as a recognized standard.
Areas Covered in the Session: Explanation of Hazard Analysis terms Hazard Analysis Process Explanation using a Template Examples of Terms will be given Hazard Analysis Examples will be Covered Step by Step
Who Will Benefit: Engineer Engineering Manager Regulatory Personnel QA
Contact Detail: Compliance4All DBA NetZealous, Phone: +1-800-447-9407 Email: support@compliance4All.com
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