GCP Announces RAPS Approved Seminar on Validation and 21 CFR Part 11 Compliance of Computer Systems at Singapore
April 7 - 8, 2014 - Singapore CA USGlobalCompliancePanel
globalcompliancepanel@gmail.com
Phone:8004479407
Fax:302 288 6884
Overview: This Interactive course to cover all areas of 21 CFR 11 and how to include 21 CFR 11 requirements in computer systems validation. Will include exercises where the attendees will build all the deliverables for a computer system using the 21 CFR 11 principles and requirements. Finally, a fun 'Jeopardy' quizzes will be used to test the participants' knowledge Why should you attend? In December 2010 the FDA changed the way it does audits to include 21 CFR 11 add-on inspections. Very little is known about this, yet the FDA has already issued citations on the subject. This Webinar will present the latest on FDA thinking (with slides directly from the FDA's Office of Compliance), discuss how these inspections will impact both your company an the industry, and provide guidance on how your company can ensure that they have a successful inspection. Course Description: Day 1 – Agenda Lecture 1: INTRODUCTION TO 21 CFR 11 • History of 21 CFR 11 • Current Status of 21 CFR 11 • 21 CFR 11 Overview • 21 CFR 11.10 (a)-(k) • 21 CFR 11.30 • 21 CFR 11.50 • 21 CFR 11.70 • 21 CFR 11.100 • 21 CFR 11.200 • 21 CFR 11.300 • The FDA's Requirements for 21 CFR 11 • FDA's Add-On Inspections for 21 CFR 11 Lecture 2: 21 CFR 11.10 (A) COMPUTER SYSTEMS VALIDATION DELIVERABLES • Risk Assessment • Vendor Audit • Validation Plan • Requirements Specification • Design Specification Day 2 – Agenda Lecture 3: 21 CFR 11.10 (A) COMPUTER SYSTEMS VALIDATION DELIVERABLES • Installation Qualification (IQ) • Operational Qualification (OQ) • Performance Qualification (PQ) • Traceability Matrix • Validation Summary Report • Validation Registry • SOPs • 21 CFR 11 Audit Lecture 4: 21 CFR 11.10 (A) COMPUTER SYSTEMS VALIDATION DELIVERABLES EXERCISE • Create ALL Deliverables for a Laboratory Information Management System (LIMS) • Jeopardy - Test Your Knowledge Who Will Benefit: • Everybody using computers in FDA or regulated environments • IT manager and staff • QA managers and personnel • Regulatory affairs • Training departments • Consultants • Validation specialists • Project Managers • Vendors of COTS (Commercial Off The Shelf) systems in regulated industries • Anyone dealing with electronic records and/or electronic signatures About Speaker: Angela Bazigos CEO, Touchstone Technologies Silicon Valley Angela Bazigos, is the CEO of Touchstone Technologies Silicon Valley, Inc. "Your Passport to Compliance". She has 30 years of experience in the Lifesciences industry spanning Project Management, Quality Assurance and Regulatory Affairs and has a patent aimed at speeding up Software Compliance. Ms Bazigos is a member of the SQA CVIC (Society of Quality Assurance Computer Validation Initiative Committee), ASQ, DIA and RAPS and consults to investment groups on Lifesciences investments as well as Pharma / Biotech / Medical Device companies on compliance matters, including strategy, submissions, quality assurance and remediations following action by the FDA. She teaches classes on Compliance, 21 CFR 11, Computer Systems Validation, and Project Management both to investor groups and industry. DATE, VENUE & PRICE: Location: Singapore| 7th & 8th April 2014| 9 AM to 6 PM Venue: Mandarin Orchard Singapore Address: 333 Orchard Road, Singapore 238867 Price: $1,595.00 Register now and save $200. (Early Bird) Until March10, Early Bird Price: $1,595.00 From March11 to April 05, Regular Price: $1,795.00 Contact Information: Event Coordinator Call: +65-3158-3448 Toll free: 1800 447 9407 Fax: 302 288 6884 Email: support@globalcompliancepanel.com Website: https://www.globalcompliancepanel.com EVENT Link – http://bit.ly/1c0kJgb LIVE CHAT SUPPORT ALSO - http://www.globalcompliancepanel.com/chat/client.php NetZealous LLC, DBA GlobalCompliancePanel, 161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA Phone: 1800 447 9407