Seminar - Online
Compliance with 21 CFR, Part 820 (the FDA’s Quality System Regulation) is not optional for device manufacturers wanting to enter medical devices into commerce in the United States. Compliance is driven, in part, by device classification (three device classes in the U.S.). However, many device manufacturers entering products into commerce for the first time struggle to understand what is actually required for compliance. If your organization is struggling with understanding the salient requirements associated with 21 CFR, Part 820, this webinar is for you. This webinar will help your organizations better understand the FDA’s expectations for implementing a Quality Management System (QMS), while providing insight into tools needed for establishing an effective approach to quality management. For establishments already having a compliant QMS, this webinar will help your organization streamline their approach to Quality Management.
Organization: Compliance Trainings (https://compliancetrainings.com)
For more information, please visit: https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=MD1446
Wednesday, July 29, 2015 (13:00 - 14:00)
Mississauga, Ontario 44813, Canada
Contact: Compliance Trainings (suzzane.d@compliancetrainings.com)
Phone: 4169154458
If you'd like to ask a question or post a comment about this talk please do so below.
This seminar posting is brought to you by Biotechnology Calendar, Inc. providing access to research information and research tools for nearly 20 years. Visit our Science Market Update Blog for current science funding and market information or see our schedule of upcoming science research laboratory product shows.
