Webinar On Developing a Quality Management System

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