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

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 management

The risk management process

Management responsibilities

Qualifications of Personnel

The Risk Management Plan (RMP) and the Risk Management File (RMF)

Elements of risk analysis

The evaluation of risk

Elements of risk control

Evaluation of residual risk

Risk Management Report (RMR)

Production and post-product information

Who Will Benefit:

Quality Professionals

Regulatory Professionals

Design Engineers

Manufacturing Engineers

Project Managers

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 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada
Customer Support : 4169154458 
Email : support@compliancetrainings.com

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https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1443

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