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Course Catalog


Click here to download our 2008 catalog.

Computer System Validation and Quality Assurance

 

Training •  Consulting  •  Readiness Audits



Software validation does not have to be a "dark and stormy night." Sure you can read the regulations.  You can even go to a class that teaches you what the regulations say.  But you are often left with an empty feeling -- "Yeah, but what am I supposed to do about computer system validation?"  That's where Praxis can help.  Our validation training combined with the power of Validation CenterTM will give you the information, hands-on experience, and tools you need to be successful.
 
Classroom Training
 
Whether you are new to computer system validation or an experienced validation engineer or QA professional, our validation training will give you the information, insight, techniques, and tools you need to be successful.
 

Level 1

Level 2

Level 3

ABCs of Computer System Validation

Computer System Validation Boot Camp®

Computer System Validation for Project Managers

Risk-Based Computer System Validation

2-day workshop
Build your essential skill set
5-day workshop
Intense emersion
from A to Z
2-day workshop
Unique focus on Project Manager roles
2-day workshop
Advanced insight into the Risk-Based approach
 
Classes are held in the Praxis Learning Centers or delivered at your location. If you have specific needs, we can customize one of our workshops just for your group. Please let us know how we can help you meet your performance goals.
 
Live E-Learning
 
Course Name Date Time
Introduction to Computer System Validation--101 September 15-16, 2008 1:00 PM -4:30 PM EDT
 
Validation CenterTM
 
Based on many years of real-world experience, continuously updated with the latest regulatory and industry trends, Validation CenterTM is your source for the information and tools you need to do Computer System Validation and Software Quality Assurance (SQA).  A standard subscription is free for 90 days with Computer System Validation Boot Camp® registration.
 
Includes:
•  CSV Templates
•  Sample SOPs 
•  FDA, EMEA, and other international regulatory news, including warning letters and FDA 483s 
•  Expert Insights into Pharmaceutical and Medical Device Industry Trends
•  Easy Access to Computer-related regulations and guidelines, including 21 CFR Part 820, 21 CFR Parts 210 and 211, 21 CFR Part 11, and many others
 
 
 
About Praxis Life Sciences

Click here to learn more about Praxis Life Sciences.
 
Contact Us
 
Click here for our complete contact info.
317.275.2870
info@praxisln.com

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