2-day In-person Seminar on Software Validation for the New FDA Inspections

Computer systems need to be compliant in relation to a few important areas. Some areas of regulation relating to implementation of computerized systems can be worked out for better results.

Fremont, CA (prHWY.com) March 25, 2013 - From: Date: 25 March 2013
NetZealous LLC,
43337| Livermore Common, Fremont| CA 94539, USA
Ph: 800-447-9407
Website: http://bit.ly/15QcPyI
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Summary: GlobalCompliancePanel to hold two-day, in-person seminar in Philadelphia on the topic, "Software Validation for the New FDA Inspections" on April 18 and 19, 2013( Thursday & Friday). David Nettleton, an FDA Compliance Specialist for 21 CFR Part 11, HIPAA, and Computer System Validation, will be the speaker at this two-day session.
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Venue: The venue for this seminar is the DoubleTree by Hilton Hotel Philadelphia Center City, Philadelphia , Pennsylvania, 19107-5686, USA
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What the seminar is about:
Computer systems need to be compliant in relation to a few important areas. Some areas of regulation relating to implementation of computerized systems can be worked out for better results.When more enhanced and effective software validation systems are put in place, an organization can save hugely on resources and time.

Helping participating organizations achieve all these is the aim of this seminar. It will help participants reduce software validation costs by as much as two thirds. During two days of high interaction studded with real life examples and proven techniques; the speaker, David Nettleton will bring the full strength of his experience in the field and detail all the requirements for 21 CFR Part 11 and HIPAA that relate to SOPs, software features, and risk-based validation.

Participants will learn how to use electronic records and electronic signatures to maximize productivity. They will also be able to prepare for an audit and will benefit IT, QA, laboratory, clinical, and manufacturing staff, as well as software vendors.
A grasp of advanced concepts such as how to "Right size" change control methods that allows quick and safe system revalidation and reducing testing time, and preparing documents that avoid 483s and warningare the other benefits of this seminar.
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About the Speaker:Founder of Computer System Validation (CSV), David Nettleton is an FDA Compliance Specialist for 21 CFR Part 11, HIPAA and Computer System Validation. His latest book, Risk Based Software Validation -Ten easy Steps, relates to the development, purchase, installation, operation and maintenance of computerized systems used in regulated applications.

An accomplished author, David has written extensively on a range of Compliance issues. He is co-author of Commercial Off-the-Shelf (COTS) Software Validation for 21 CFR Part 11 Compliance (Davis Horwood International and PDA - www.pda.org), and Electronic Record Keeping; Achieving and Maintaining Compliance with 21 CFR Part 11 and 45 CFR Parts 160, 162, and 164 (Interpharm/CRC - www.crcpress.com).

The seminar:
This is the agenda of this seminar:

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
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For whom:
This seminar will benefit professionals in/amongthe following areas:
o IT
o QA
o QC
o Laboratory staff
o Managers
o Regulatory Affairs
o GMP, GCP, GLP professionals
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About GlobalCompliancePanel:
GlobalCompliancePanel (GCP) is a specialized offering from NetZealous LLC, a Technology and Business Process Solutions and Services Company registered in Fremont, CA. It is a fountainhead for Continuous Professional Education, compliance training and consulting. GCP offers a broad range of high quality regulatory and compliance-related services relating to Medical Devices, Pharmaceutical, FDA, Food, PCI industries, and SOX. Some of the Governing Areas its webinars cover are GxP (Manufacturing / Clinical / Lab), EU and ISO.

These seminars are an extension of online trainings, at which GCP has conducted around 700 webinars since inception on a variety of topics for these industries /verticals. More than 30,000 professionals have benefited from these trainings. GlobalCompliancePanel's trainings are focused, flexible and tailored to the client's need.

This is the next in a series of regulatory and compliance related seminars that GlobalCompliancePanel has been organizing all over the US. Its previous seminars have met with resounding success. GlobalCompliancePanel's seminars have helped participants reach their career milestones. In bringing globally renowned experts in the field of regulatory compliance and executives in the industry together, GlobalCompliancePanel fosters a learning experience. With trainings that are focused and relevant, GlobalCompliancePanel seeks to serve as a bridge in the area of continuous professional education for regulatory and compliance-related fields.
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Price: $1,295.00
Register now and save $200. (Early Bird)
Until March 29, Early Bird Price: $1,295.00
From March 30 to April 23, Regular Price: $1,495.00
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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
43337 Livermore Common, Fremont CA 94539, USA

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Tag Words: hipaa seminar, software validation, compliance seminar, fda inspections, us conference, us seminar

Categories: Health

Press Release Contact
USA
GlobalCompliancePanel,
Livermore Common, Fremont,
CA 94539, USA Phone: 1800 425 9407

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