Compliance Trainings, Online
2015-07-15
Description : This webinar provides an overview of the Quality Management System requirements. We will discuss ISO Quality Management standards and the FDA Quality System requirements. Medical device companies are utilizing ISO standards to build their business management systems because of their benefits and as a necessary step to market their products globally. During this webinar we will discuss the documentation process, and implementing a management system to meet the requirements of ISO and QSR and the operational objectives of the company. This course will provide guidance on best practices for developing a compliant QMS. We will explore strategies for dealing with common documentation and compliance issues. The course also summarizes the essential documentation requirements and gives an introduction to the key elements for implementation of a compliant system. Areas Covered in the Session : By the end of this course, participants will have a understanding of: Understand the Quality Management Principles Discuss the benefits of an effective QMS Review the Quality Essentials Procedure Development Understand the required documentation: Quality Manual Policies Procedures Work Instructions Identifying Exempt sections & how to document Managing and maintaining your QMS Who Will Benefit: Quality Associates New Quality Assurance Managers ISO 13485/9001 Implementation Team Members, Management Representatives For more information and enquiries contact us at Compliance Trainings 5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada
Customer Support : #416-915-4458
Email : support@compliancetrainings.com
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