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Webinar On Implementing Adequate CAPA and Design Control Procedures

Device firms, who are intending to bring medical device products into the US market, are subject to quality system regulations.

Description :Device firms, who are intending to bring medical device products into the US market, are subject to quality system regulations.Recent FDA enforcement trends (including 2013) reveal that both design control and Corrective and Preventive Action (CAPA) systems are critical elements to sustain FDA inspections.Device manufacturers are required to establish and maintain FDA-compliant quality management systems, where appropriate and applicable, including design control and CAPA systems. This webinar is intended to provide guidance on understanding, interpreting, and implementing design control and CAPA system requirements.  This presentation is further intended to help you establish and maintain adequate design control and CAPA procedures for all classes of medical devices including IVDs.Understanding, interpreting, and implementing design control and CAPA system requirements in a holistic manner can significantly contribute to your product quality and regulatory compliance, helping to ensure your innovative medical products to be safe and effective on a global market and saving enormous amount of your unnecessary time, efforts and investment.This 60-min webinar will provide great opportunities for you to get familiar with regulatory and quality requirements for design control and CAPA systems applicable to all types of medical devices including IVDs.This webinar is intended to help you learn and ensure you can implement adequate CAPA and design control procedures. In addition, this webinar will provide an opportunity to better understand and adequately implement adequate design control and CAPA systems.Areas Covered in the Session :Applicable Laws and RegulationsStatutory and Regulatory RequirementsIntroduction and DefinitionsDesign and Development PlanningDesign Input and Design OutputDesign ReviewDesign Verification And ValidationDesign Transfer and Design ChangesDesign History File (DHF), Device History Record (DHR) and Device Master Record (DMR)Corrective and Preventive Action (CAPA)Root Cause AnalysisCAPA ElementsCommon ProblemsHow to Avoid Common MistakesSpeaker’s Recommendation and Suggestions on PASS-IT SolutionsWho Will Benefit:CEOsVPsCompliance OfficersClinical Affairs (Associates, Specialists, Managers, Directors and VPs)Regulatory Affairs (Associates, Specialists, Managers, Directors and VPs)Quality Assurance (Associates, Specialists, Managers, Directors and VPs)R&D (Engineers, Scientists, Managers, Directors and VPs)CROsConsultantsContractors/Subcontractors

When

22 Oct 2015 @ 12:00 pm

22 Oct 2015 @ 02:00 pm

Duration: 2 hours

Timezone: GMT -5:00


Where

Online Webinar


Organised by

Compliance Trainings (deactivated)

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