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  • This course will teach you how to reduce software validation costs by as much as two thirds.
  • It details all the requirements for 21 CFR Part 11 and HIPAA that relate to SOPs, software features, and risk-based validation.
  • The course is highly interactive, using real life examples and proven techniques.
  • You will learn how to use electronic records and electronic signatures to maximize productivity.
  • This course will teach you how to prepare for an audit and is intended for IT, QA, laboratory, clinical, and manufacturing staff, as well as software vendors.
  • The instructor starts with the basics and covers advanced concepts such as how to "Right size" change control methods that allows quick and safe system revalidation.
  • Learn how to reduce testing time, and how prepare documents that avoid 483s and warning letters.

Course Outline:

Day 1 – Agenda

Lecture 1: Introduction to the FDA

Lecture 2: 21 CFR Part 11 - Compliance for Electronic Records and Signatures

Lecture 3: HIPAA Compliance for Electronic Records

Lecture 4: The Five Keys to COTS Computer System Validation

Lecture 5: The Validation Team

Day 2 – Agenda

Lecture 6: Ten-Step Process for COTS Computer System Validation

Lecture 7: How to Write Requirements and Specifications

Lecture 8: How to Conduct a Hazard Analysis/Risk Assessment-Exercise

Lecture 9: Software Testing

Lecture 10: System Change Control

Lecture 11: Cost Reduction Without Increasing Regulatory or Business Risk

Lecture 12: Q & A Lecture 12: Q & A

Who Will Benefit:




Laboratory staff


Regulatory Affairs

GMP, GCP, GLP professionals

About Speaker - David Nettleton is an FDA Compliance Specialist for 21 CFR Part 11, HIPAA, and Computer System Validation. His latest book is Risk Based Software Validation - Ten easy Steps. It relates to the development, purchase, installation, operation and maintenance of computerized systems used in regulated applications. 

He specializes in performing gap analysis, remediation plans, SOP development, vendor audits, training, and project management. He has completed more than 225 mission critical software validation projects.


Location: Bangalore | July 8th and 9th, 2013 | 9 AM to 6 PM

Venue: Vivanta by Taj 
41/3, Mahatma Gandhi Road, Trinity Circle, Bangalore, Karnataka 560001

Price:  Rs 18,000

Register now and save 2000 (Early Bird)

Until May 18, Early Bird Price: Rs 18,000.

From May 19 to June 30, Regular Price: Rs 20,000.

Contact Information:

Event Coordinator

Toll free:  +91 80-3247-3694, +91 80-3201-4957

Fax:  302 288 6884



Event Link -


NetZealous Services India Pvt. Ltd.

4th Floor, 'A' Block, Brigade Software Park,

Banashankari 2nd stage,

Bangalore - 560070 INDIA.

Contact the event managers listed below for more information about how you can participate at the 2-day In-person Seminar On Software Validation For The New FDA Inspections At Vivanta By Taj, Bangalore.

All information in Events In America is deemed to be accurate at the time we add it, and we take steps to verify all details and update our records when new information is provided, but as people, events and circumstances change, we caution users to independently confirm all information. and Events In America LLC make no guarantee of accuracy and assume no liability for inaccurate information.

Conference/Event Dates: 07/08/2013 - 07/09/2013
Conference/Event Hours: 9:00AM
Classification: B2B
Primary Industry: Software
Other Industries: Business, IT, Manufacturing, Medical, Medical Business & Administration, Software, Technology
Venue: Vivanta by Taj
Venue Type: Indoor - Hotel
Conference Hotel URL:official hotel URL
Show Owner:GlobalCompliancePanel

Booth Size Booth Cost   Available Amenities
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  Water: n/a
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Other Booth Sizes Available: n/a

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2-day In-person Seminar On Software Validation For The New FDA Inspections At Vivanta By Taj, Bangalore

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