Thu, Apr 27, 2017, 02:30 PM - Fri, Apr 28, 2017, 11:30 PM
We have all heard of Data Integrity but do you really understand what it is? Do you understand how 21 CFR 11 and Annex 11 fit into this picture? Specifically, can you answer questions on the following?
I often refer to 21 CFR 11 and Annex 11 as Good Software Engineering with the Documentation on Steroids! However, unless one knows how to implement Data Integrity, it is often very hard to apply requirements for DATA INTEGRITY to computerized system, and very hard to determine what needs to be done, to meet domestic and / or international regulations or business continuity requirements. In addition, the agencies have stepped up data integrity inspections and the number of citations on the subject is skyrocketing!
This course is appropriate for beginner and experienced person alike. The topics will build on each other and will give you the latest trends in our heavily regulated industry and how to make it easy for yourself while still achieving data integrity.
This is a very hands-on class and the attendees will be given take away templates that will enable them to build a complete package to meet Data Integrity Requirements for Computerized Systems
This Hands-On course will provide the attendees with more detailed experience on validation / 21 CFR 11 compliance of a computer system, as well as details for activities associated with computer systems validation as follows:
1. What is Data Integrity and how is it implemented
2. How to use Risk Based Assessments to reduce work while still achieving Data Integrity and Compliance?
3. Data Integrity Frequently Asked Questions
4. Validation Master Plan
5. Risk Based Assessment
6. Complete Validation for a System (software development lifecycle)
7. Automated Test Tools
8. Infrastructure Requirements
9. Change Control
Who will benefit:
Day 1 Schedule
Day 1 Schedule
Introduction / Background
21 CFR 11 & Annex 11
Risk Assessment & Requirements
Day 2 Schedule
Verification & Testing
Change Control & SOPs
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.
More recently, Ms. Bazigos co-authored Computerized Systems in Clinical Research / Current Data Quality and Data Integrity Concepts with FDA, DIA and Academia. She is on the board for UC Berkeley's Business School for Executive Education in Life Sciences and on the Stanford Who's Who Registry for contributions to the Lifescience industry.
Location: Mumbai, India Date: April 27th & 28th, 2017 and Time: 9:00 AM to 6:00 PM
Venue: The LaLiT Mumbai
Address: Sahar Airport Road, Andheri East, Mumbai - 400059
Register now and save ₹ 2000. (Early Bird)
Price: ₹ 14,000 (Seminar for one Delegate)
Until March 25, Early Bird Price: 14,000 From March 26 to April 25, Regular Price: 16,000
NetZealous - GlobalCompliancePanel
NetZealous Services India Pvt. Ltd.
Gururaya Mansion, 759 to 764, 8th Main road, J.P.Nagar,
Bangalore - 560078 Karnataka, INDIA
Phone: 1800 425 9409
Registration Link – https://www.globalcompliancepanel.in/control/FDA-data-integrity-21-CFR-11-Mumbai
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