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Webinar On Application of Risk Management in Accordance with EN ISO 14971:2012

FDA Risk Management

Description : All industry professionals, regardless of functional roles, will benefit from this training, especially if you are involved in the day-to-day activities associated with your organization’s product development or manufacturing operations. The application of risk management is a salient requirement needed for introducing medical devices that are safe and effective in their intended use.Areas Covered in the Session :General requirements for risk managementThe risk management processManagement responsibilitiesQualifications of PersonnelThe Risk Management Plan (RMP) and the Risk Management File (RMF)Elements of risk analysisThe evaluation of riskElements of risk controlEvaluation of residual riskRisk Management Report (RMR)Production and post-product informationWho Will Benefit:Quality ProfessionalsRegulatory ProfessionalsDesign EngineersManufacturing EngineersProject ManagersPrice Tags:LiveSingle Live : For One Participant$ 249Corporate Live : For Max. 10 Participants$ 899RecordingSingle REC : For One Participant - Unlimited Access for 6 Months$ 299For more information and enquiries contact us atCompliance Trainings5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada Customer Support : 4169154458 


13 Feb 2015 @ 01:00 pm

13 Feb 2015 @ 02:00 pm

Duration: 1 hours

Timezone: GMT -5:00


Online Webinar



Organised by

Compliance Trainings (deactivated)

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