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Webinar On Building a Compliant Documentation and Training System
1/26/2015 1:00 PM - 2:00 PM
Online Mississauga, Ohio Canada
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Summary:

This 60 minutes webinar will give a better understanding of the relationship between compliance, documentation, and training. It will provide participants with the ability to effectively meet regulatory requirements, properly integrate training into their quality system, and develop effective compliance documentation that meets both regulatory and training purposes.

Webinar On FDAs New Enforcement of 21 CFR Part 11
1/15/2015 1:00 PM - 2:15 PM
Online Mississauga, Ohio Canada
Event Listing
Summary:

The seminar will have the answers. And using industry proven case studies on how to avoid 483 inspectional observations and warning letters attendees will learn how to prepare their organization for trouble-free Part 11 related inspections.

Webinar On Key Factors to Write an Effective Standard Operating Procedure SOP and Work Instruction
1/13/2015 1:00 PM - 2:30 PM
Online Mississauga, Ohio Canada
Event Listing
Summary:

This webinar will show you how to write, organize, and maintain SOPs and train personnel in a way that will ensure compliance in a way that is concise, reproducible and easy to follow.

Webinar On US FDAs Strategic Priorities 2015 and Beyond
1/21/2015 1:00 PM - 2:30 PM
Online Mississauga, Ohio Canada
Event Listing
Summary:

This webinar will discuss about two “Strategic Priorities” that the FDA has published to emphasize their future directions vis a vis regulated industry and public safety.

Webinar On What is the harm in that Risk Management 101
1/22/2015 1:00 PM - 2:00 PM
Online Mississauga, Ohio Canada
Event Listing
Summary:

A Highly regarded talk during recently held ASQ World Conference on Quality and Improvement. This course is meant to be a needed introduction to risk management for a broader range of professionals.

Webonar on Design Inputs Design Outputs Traceability Matrix Principles of Lean Documents
1/21/2015 1:00 PM - 2:30 PM
Online Bakersville, Ohio Canada
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Summary:

In this webinar, we apply the Theory of Lean documents and its corollary Theory of Lean Configuration to present a fresh approach to these linked and cascading documents.

Webinar On The FDA Drug Approval Process
1/15/2015 1:00 PM - 3:00 PM
Online Mississauga, ON Canada
Event Listing
Summary:

This web seminar provides an overview of the entire FDA Drug Approval Process. This seminar will cover FDA requirements from discovery.

Webinar On How to Develop a Master Validation Plan
1/27/2015 1:00 PM - 2:00 PM
Online Mississauga Canada
Event Listing
Summary:

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.

Webinar On FDA proposed changes to ISO 13485 2015 and Medical Devices Quality Management Systems
1/30/2015 1:00 PM - 2:30 PM
Online Mississauga Canada
Event Listing
Summary:

You will gain a thorough insight into the specific auditing requirements of the International ISO 13485 Standard requirements for medical devices. This class will truly build your knowledge from the fundamental principles and help you grow into fulfilling the regulatory requirements as a product developer, manufacturer, auditee for external FDA type of audits and serve as an internal or supplier auditor

Webinar On Statistical Process Control SPC
1/20/2015 1:00 PM - 2:00 PM
Online Mississauga Canada
Event Listing
Summary:

SPC continually adjusts its sensitivity in order to ensure that such investigations are performed only when there is a reasonable chance of identifying causes of variation

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