COMPLIACNE TRAININGS 2014 - Webinar On - ICH Q10 Pharmaceutical Quality System

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Category Compliance Trainings, Medical Device, Regulatory Affairs, FDA, Pharmaceuticals, online training, Healthcare, Regulatory Compliance, ICH Q10, GMPs,QSA, ICH Q10-10

Deadline: February 05, 2014 | Date: February 05, 2014

Venue/Country: Online, Canada, Canada

Updated: 2013-12-26 15:43:48 (GMT+9)

Call For Papers - CFP

ICH Q10 is particularly important because the USA, Canada, Europe, and Japan have announced their intentions to adopt the ICH Q10 guidance. Therefore, it is necessary to understand and comply with this guidance in order to market your products across international boundaries. However, there is another and probably more important reason. The reason being that this guidance has some very useful quality concepts that have the potential to help maintain and improve your quality system for improving compliance and increasing customer satisfaction. For greater insight about maintaining and improving quality systems, review the FDA's “Quality Systems Approach to the Pharmaceutical GMPs”

This webinar provides a broad overview of ICH Q10, The Pharmaceutical Quality System. ICH Q10 is applicable throughout the pharmaceutical lifecycle. Unlike the FDA Quality Systems Approach limited applicability, ICH Q10 explains the application of quality principles and concepts to the regulations. The ICH Q10 concepts will be presented in a logical sequence that will show their applicability to the pharmaceutical product lifecycle to strengthen the link between pharmaceutical development and manufacturing activities.

This webinar focusses on The Quality Systems Approach (QSA) To Pharmaceutical Good Manufacturing Practices. The focal point of the QSA is drug substances and products but its principles apply to all FDA regulated industry. This guidance is written in a non-regulatory format explaining GMP concepts in a practical and easily understood way. This webinar uses many graphical aids to increase interest and enhance training.

Middle and Senior Management from all functions involved in establishing and executing corporate strategy and objectives. It is particularly applicable to companies new to the FDA regulated industry.

Senior quality management will gain insight on how quality systems work and will be able to better understand senior management responsibilities. Provide knowledge that can be used to persuade others concerning quality matters.

Finance, Sales and Marketing, Operations, Procurement, and Human Resources who have an active or supporting role in Quality.

Other quality personnel who have the desire and/or potential to advance to quality leadership.

Areas Covered in the Session :

? Course Introduction, Objectives, & Quality Philosophy

? Defining the Role of Quality and Compliance in the Organization

? Why does ICH Q10-10, Pharmaceutical Quality Systems, Exist? Introduction, Scope & Objectives

? Arrangement & Organization of the ICHQ 10 Guidance

? Relationship to other regulatory requirements & regional regulations

? Enablers-Knowledge, Risk, & Design Management

? Introduction to the Pharmaceutical Product Lifecycle

? First Introduction to the Quality Manual

? Management Responsibility

? Pharmaceutical Quality System Elements

? Continual Improvement of Process Performance & Product Quality

? Continual Improvement of the Pharmaceutical Quality System

? Regulatory Body Enforcement

? Quick Review

? Q&A

Who Will Benefit:

? Middle and Senior Management

? Companies new to the FDA regulated industry

? Quality Assurance

? Quality Control

? Regulatory Affairs

? Senior quality management

? Compliance Director

? Vice Presidents

? Consultants

? Project Leaders

? Research & Development

? Sales and Marketing, Finance & Cost Accounting, and Procurement Departments

? Operations Department

? Human Resources who have an active or supporting role in Quality

? Other quality personnel who have the desire and/or potential to advance to quality leadership

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