Seminar - Online
This webinar will provide valuable assistance to all U. S. FDA-regulated companies. It will assist in their reviewing and modifying their regulatory compliance stance in view of the areas the FDA indicates are of growing / future interest / emphasis. Its principles apply to personnel / companies in the Medical Devices, Pharmaceutical, Diagnostic, and Biologics fields Areas Covered in the Session : FDA Device Clearance / Changes in Direction Current Design Control Requirements Defining the "Start" Date and Its Significance The 9 Design Control Elements and Their Implementation and Documentation "Retroactive" Design Control “Agile” Design Control The Business Case for Design Control Interactive Q & A session Who Will Benefit: The employees who will benefit include: Senior management Middle management R&D Engineering Software QA / RA Manufacturing Operators Consultants cGMP instructors And all personnel involved in verification and/or validation planning, execution and documentation.
Organization: Compliance Trainings (https://compliancetrainings.
For more information, please visit: https://compliancetrainings.
com/SiteEngine/ ProductDetailView.aspx?id= MD1543
Tuesday, June 23, 2015 (13:00 - 14:00)
Mississauga, Ontario 43717, Canada
Contact: Compliance Trainings (suzzane.d@compliancetrainings.
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