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Webinar On Preventing Medical Device Recalls

 
  October 01, 2015  
     
 


Compliance Trainings, Mississauga
2015-10-26


Description :

The secret to preventing medical device recalls is to implement and follow basic practices for specifications and design control, design for process reliability, production validation and design validation using accelerated life tests. This webinar is about controlling safety risk from specification writing to device retirement – control throughout the product’s life cycle.

In a recent study, the FDA has reported a 95% increase in medical device recalls over a nine year period ending in 2014 attributable to a variety of reasons. Whatever the reason, medical device recalls are expensive and most importantly carry significant risk to the health and safety of patients.

The increase indicates serious failures in the processes and controls designed to ensure reliability, safety, and effectiveness of the recalled devices. As medical devices become more complex and software components become more critical to device functioning, the need for proactive risk prevention becomes more and more evident.

The webinar will provide an overview and a foundation for further learning concerning preventing recalls during specification writing, risk assessment and risk management, preventing recalls during the early design and the detail design phases of development, and preventing recalls during validation, verification, and software design.

Areas Covered in the Session :

Preventing recalls during specification writing

Preventing recalls during early design

Preventing recalls during the detail design phase

Designing for Prognostics to protect patients

Preventing recalls during production validation

Preventing software design recalls

Preventing supply chain quality defects to avoid recalls

Preventing recalls using a verification process

Preventing recalls using the design validation process

Role of management in preventing recalls

Innovative methods useful in preventing recalls

Who Will Benefit:

Quality Professionals

Regulatory Professionals

Manufacturing & Design Engineers

Compliance Departments

Research & Development Teams

Documentation Personnel

Complaint Handling Personnel

 

Product Development Teams

 
 
Organized by: Compliance Trainings
Invited Speakers:

Charles Paul is an instructional designer and management consultant with over 30 years’ experience providing training and consulting services to regulated industries. He has installed quality systems and designed and developed GMP and operational documentation and training programs for foods and beverage, pharmaceuticals, biotech, cosmetics, and consumer product – OTC industries.

 
Deadline for Abstracts: 2015-10-26
 
Registration:

For more information about this event please visit

 

https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=MD1467

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

To register this webinar 

E-mail: suzzane.d@compliancetrainings.com
 
   
 
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