Netzealous LLC DBA - Compliance4All, Online
2018-08-28
Overview: It is not about giving an OK to products, it is about trusting the manufacturer to do the right thing. Overall, your regulatory approach to software regulation needs to ease up and reap the benefits where they apply. Your company may even save money, a nice benefit.
Why should you Attend: The scope of your program should be re-evaluated to identify your least burdensome approach. You can learn what matters and what does not. You can implement faster ways to move products into the marketplace and decide whether or not you want to involve FDA in your cybersecurity problems. You can prepare now to qualify for the new Digital Health initiative, but you have homework to do first.
Areas Covered in the Session: 21st Century Cure Act Impact Software no longer under FDA jurisdiction Changes in premarket requirements Voluntary controls short cuts Postmarket reporting options Digital Health Initiative - FDA clearance not required
Who Will Benefit: Regulatory Affairs Directors Software Designers / Specification Developers Production Managers Quality Assurance Directors In-House Legal Counsel
Event Fee: One Dial-in One Attendee Price: US $150.00
Contact Detail: Compliance4All DBA NetZealous, Phone: +1-800-447-9407 Email: support@compliance4All.com
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