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Event
19 Sep 2013
Trade

2-day In-person Seminar on

This Seminar will teach you how to reduce software validation costs by as much as two thirds. The Seminar is highly interactive, using real life examples and proven techniques.

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 – AgendaLecture 1: Introduction to the FDALecture 2: 21 CFR Part 11 - Compliance for Electronic Records and SignaturesLecture 3: HIPAA Compliance for Electronic RecordsLecture 4: The Five Keys to COTS Computer System ValidationLecture 5: The Validation TeamDay 2 – AgendaLecture 6: Ten-Step Process for COTS Computer System ValidationLecture 7: How to Write Requirements and SpecificationsLecture 8: How to Conduct a Hazard Analysis/Risk Assessment-ExerciseLecture 9: Software TestingLecture 10: System Change ControlLecture 11: Cost Reduction Without Increasing Regulatory or Business RiskLecture 12: Q & AWho Will Benefit:ITQAQCLaboratory staffManagersRegulatory AffairsGMP, GCP, GLP professionalsSpeaker 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 PDTHotel: 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: $1,295.00From August 01 to September 17, Regular Price: $1,495.00 Contact Information: Event CoordinatorToll free: 1800 447 9407Fax: 302 288 6884GlobalCompliancePanelNetZealous LLC161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA

When

19 Sep 2013 @ 09:00 am

20 Sep 2013 @ 06:00 pm

Duration: 1 days, 9 hours


Where

Doubletree Hotel San Diego Downtown

1646 Front Street

Little Italy

United States


Language

English en


Organised by

GlobalCompliancePanel (deactivated)

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