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Webinar on Conducting a Documentation and Training Analysis

 
  August 07, 2015  
     
 


Compliance Trainings, Online
2015-08-12


This webinar will provide the best practice approach for conducting an efficient, effective, and complete documentation and training analysis for a regulated environment as well as developing both training materials and compliance documents that effectively serve a multitude of uses. How well an analysis is conducted impacts cost, the speed of training delivery, and the quality of the regulatory documentation produced.

This webinar will guide the participant through the entire process from start to finish and will discuss how training materials and compliance documentation can be developed to meet complimentary purposes.

Areas Covered in the Session :

Elements of a regulatory documentation and training program

How regulatory documentation and training are linked

Regulatory compliance documentation hierarchies

Areas of the organization/process that must be examined and analyzed

Conducting the analysis – using subject matter experts

Training task characteristics that impact training delivery

Use of the Analysis Tool to capture the required information

Performance objectives, how they are developed and how they impact the training process

Who Will Benefit:

A must attend webinar for all personnel / companies in the Pharmaceuticals, Medical Devices, Biotechnology, Cosmetics, Personal Products, Foods & Beverages fields. The professionals who will benefit include all:

Training Managers and Directors

Regulatory Affairs

Quality Professionals

Documentation department

Compliance officer

Product Development Professionals

QA/QC analysts

Manufacturing Teams

Production Teams

Operations

 

Consultants

 
 
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: 2015-08-11
 
Registration:

For more information about this event please visit

 

https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1466

E-mail: suzzane.d@compliancetrainings.com
 
   
 
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