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Webinar on Risk Management - Principles of Lean Documents and Lean Configuration

 
  March 04, 2016  
     
 


Compliance Trainings, Online
2016-04-06


Description :

Risk management is a process that involves many considerations, responsibilities, personnel, and the transfer of knowledge. Given that it transcends projects and even companies, it is particularly critical that key pieces of information survive these many hand-offs.

"The new standard expects you to apply a 'risk based approach' to your organization's QMS processes. The old standard also expected you to think about risk, but only during product realization (in section 7).

Now, you're expected to apply risk management methods and techniques to all QMS processes, including outsourced processes."

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, files, and requirements.

If you are constantly struggling to create, manage, and maintain all of the information found in the various Risk Management documents and files, all of which are often redundant, repetitive, and clustered together in an awkward manner, this webinar is something that will give you a different perspective and a very different approach that you can use.

If your design and manufacturing resources are spending too much time on documentation and not enough time on actual risk management and mitigation, you as a manager need to be looking for ways to simplify the work at hand.

This webinar presents a new approach yet is based on solid principles and proven practices.

Areas Covered in the Session :

Brief introduction to Lean Documents and Lean Configuration

Risk management process as per ISO 14971

Management responsibilities

Qualification of personnel

Risk management plan

Risk management file

Bringing it all together – links to design and process

Who Will Benefit:

All Managers, Supervisors, Directors, and Vice-Presidents in the areas of:

Research & Development

Design Assurance

Quality Assurance

Operations

Document Control

 

Manufacturing Engineering

 
 
Organized by: Compliance Trainings
Invited Speakers:

José Mora is a Principal Consultant specializing in Manufacturing Engineering and Quality Systems. For over 30 years he has worked in the medical device and life sciences industry specializing in manufacturing, process development, tooling, and quality systems. Prior to working full time as a consulting partner for Atzari Consulting, José served as Director of Manufacturing Engineering at Boston Scientific and as Quality Systems Manager at Stryker Orthopedics, where he introduced process performance, problem solving, and quality system methodologies. During that time he prepared a white paper on the application of lean manufacturing methods to the creation and management of controlled documents and a template for strategic deployment.

 
Deadline for Abstracts: 2016-04-06
 
Registration:

For more information about this event please visit

https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=MD1940

 

To register this webinar

https://compliancetrainings.com/siteengine/Login.aspx 

E-mail: suzzane.d@compliancetrainings.com
 
   
 
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