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Online Webinar
27 Jan 2015
Science

Webinar On How to Develop a Master Validation Plan

Every medical device company (OEM) must meet certain standards for validation of its transfer plans, facilities, clean rooms and processes. These standards apply for OEM

On Going Christmas Offers: Offer valid till 1 st January 20151. Register an attendee for Single Live:Get 10% of on every RegistrationFirst 10 attendees will receive recording Access to the webinar for No Additional CostFor Coupon Code call customer support 41691544582. Register your Group for Corporate Live:Get 15% of on every RegistrationEvery group registrant will receive Recording Access to the webinar for No Additional CostFor Coupon Code call customer support 416-915-44583. Unlimited viewing for 4 days4. The discounted amount will appear after entering the Coupon Code in the Secure Check Out PageDescription:Every medical device company (OEM) must meet certain standards for validation of its transfer plans, facilities, clean rooms and processes. These standards apply for OEM’s and suppliers to OEM’s. Many medical companies have never had a Master Validation Plan for their facilities, processes or suppliers. This is an important standard to have when being audited to show on big picture compliance to FDA and foreign standards.This webinar on “How to Develop a Master Validation Plan” (also known as Validation Master Plan) will provide a step-by-step procedure for all medical device companies and their suppliers that are in need of developing a plan for product/equipment transfer, facilities, processes or to develop a company standard.Areas Covered in the Session :Master Validation Plan contentRevision historyBackgroundObjectivePurposeScopeProject approachKey activitiesProject organizationCommunication planQuality AssuranceFacility approachValidation approachScheduleBudget ...and moreWho Will Benefit:OEM Senior managementSupplier Senior managementManagers and directorsManagers setting up new facilities and product linesPlant and facility managersEnd-users responsible for design control and product developmentR&D and product developmentProject managersFacility and clean room designersProcess engineers and managersValidation engineersQuality management and engineersAuditorsSuppliers to medical OEM’sConsultantsPrice 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 : 416-915-4458 

When

27 Jan 2015 @ 01:00 pm

27 Jan 2015 @ 02:00 pm

Duration: 1 hours

Timezone: GMT -5:00


Where

Online Webinar


Language

English en


Organised by

Compliance Trainings (deactivated)

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