2014 - Webinar On DeNovo Classification Process

This webinar provides information on FDA’s DeNovo classification process. The webinar explains how a device classified as a Class III device but has the risk level of a Class I or II device may be downclassified to its correct risk classification. The webinar will cover when the DeNovo process may be used, information contained in a DeNovo request, the 2 DeNovo pathways and FDA review process for DeNovo.
This is a must attend session for those personnel that require an understanding of the FDA’s DeNovo Classification process.
Areas Covered in the Session :
FDA DeNovo Classification Process
Request for DeNovo application
2 DeNovo Pathways
FDA DeNovo Review Process
Interactive Q&A Session
Who Will Benefit:
Regulatory Affairs Personnel
Quality Personnel
Clinical Personnel
Research Personnel
Laboratory Personnel
Manufacturing Personnel
Legal Personnel
Clinical Research Associates
Personnel who require a general understanding of the FDA’s DeNovo Classification Process
Price Tags:
Live
Single Live : For One Participant
$ 249
Corporate Live : For Max. 10 Participants
$ 899
Recording
Single REC : For One Participant - Unlimited Access for 6 Months
$ 299
For more information and enquiries contact us at
Compliance Trainings
5939 Candle brook Ct, Mississauga, ON L5V 2V5, Canada
Customer Support: 416-915-4458
Email: support-AT-compliancetrainings.com
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