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POST ID: 5622

Webinar on Quality System Regulations (QSRs) for Medical Devices and IVDs

Region: Canada
Location: Mississauga, ON
Email: suzzane.d@compliancetrainings.com
Website: http://tinyurl.com/psz32rb

Description:

This 60-min webinar will help you ensure if you engage in the best practices for establishing and maintaining quality management systems necessary to achieve compliance and to remain compliant with 21 CFR Part 820 (cGMPs).
Areas Covered in the Session:
Applicable Laws
FDA Quality System Regulations
Definitions
Design Control: Design And Development Planning, Design Input, Design Output, Design Review, Design Verification, Design Validation, Design Transfer, And Design Changes
Design History File (DHF)
Quality System Procedures, Purchasing Controls And Servicing
Who Will Benefit:
CEOs
VPs
Compliance Officers
Attorneys
R&D and Manufacturing Managers
Managers (RA, QA/QC, CA)
Consultants
Contractors and Subcontractors
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 enquiries and more contact us
Compliance Trainings
5939 Candlebrook Ct,
Mississauga, ON L5V 2V5,
Canada
Customer Support : #416-915-4458
Email : support@compliancetrainings.com


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