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2day Inperson Seminar on Software Validation for the New FDA Inspections in San Diego

9/19/2013 9:00 AM - 9/20/2013 6:00 PM

Overview:

• 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 Description:

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

Who Will Benefit:

• IT

• QA

• QC

• Laboratory staff

• Managers

• Regulatory Affairs

• GMP, GCP, GLP professionals

Speaker Profile:

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.

Date, Venue and Time:

Location: San Diego | September 19th & 20th, 2013 (Thursday & Friday) | 9 AM to 6 PM PDT

Hotel: Doubletree Hotel San Diego Downtown

Address: 1646 Front Street, San Diego, California, 92101, USA

Price: Seminar for One Delegate

$1,295.00 September 19th & 20th, 2013 (Thursday & Friday)

Discount: Register now and save $200. (Early Bird)

Until July 31, Early Bird Price: $1,295.00

From August 01 to September 17, Regular Price: $1,495.00

Contact Information:

Event Coordinator

Toll free: 1800 447 9407

Fax: 302 288 6884

Email: support@globalcompliancepanel.com

Website: https://www.globalcompliancepanel.com

LIVE CHAT SUPPORT ALSO - http://www.globalcompliancepanel.com/chat/client.php

GlobalCompliancePanel

NetZealous LLC

161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA

For More Details: http://bit.ly/13XS4Vo

Learn More: 2day Inperson Seminar on Software Validation for the New FDA Inspections in San Diego

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