2-day In-person Seminar
Data Integrity Workshop: FDA Requirements and Implementation
Time: 9:00 AM to 6:00 PM
Venue: Hilton Zurich Airport
**Please note the registration will be closed 2 days (48 Hours) prior to the date of the seminar.
The Problem:
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:
- Evolution of 21 CFR Part 11 and Annex 11 and Why they are Back in the News
- Overview and Key Requirements of Part 11 & Annex 11
- How to use a Risk Based Assessment to reduce work while still achieving Data Integrity and Compliance?
- How FDA & other Regulatory Authorities Inspect Computerized Systems for Data Integrity?
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 are 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
The Seminar:
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:
- What is Data Integrity and how is it implemented
- How to use Risk Based Assessments to reduce work while still achieving Data Integrity and Compliance?
- Data Integrity Frequently Asked Questions
- Validation Master Plan
- Risk Based Asssessment
- Complete Validation for a System (software development lifecycle)
- Automated Test Tools
- Infrastructure Requirements
- Change Control
- SOPs
Who Should Attend:
- VP of IT
- Director of IT
- Quality Managers
- Project Managers (for DATA INTEGRITY / IT)
- Validation Specialists
- Database Administrators
- System Administrators
- Directors / Senior Directors of Discovery
- Directors / Senior Directors of Development
- Directors / Senior Directors of Commercialization
- Document Managers
- Training Managers
- Consultants
- Data Managers
- Safety Managers
Day 1 Schedule
Lecture 1:
Introduction / Background
- Introductions / Participants' Understanding
- Participants' Objectives for the Course (Please come prepared to discuss)
Lecture 2:
Data Integrity
- What is Data Integrity
- How is it implemented
- Data Integrity Frequently Asked Questions
Lecture 3:
21 CFR 11 & Annex 11
- 21 CFR 11
- Annex 11
- 21 CFR 11.10(a) - Computer Systems Validation
Lecture 4:
Risk Assessment & Requirements
- Risk Assessment for Requirements
- Gathering Requirements
- Entity Relationship Diagram
- Process Decomposition
- Exercise on how to create Requirements
Day 2 Schedule
Lecture 1:
Design
- Design Specifications
- Software Configuration and Build
- Exercise on how to create Design Specifications
Lecture 2:
Verification & Testing
- Traceability Matrix
- Verification and Testing
- Other Documents
Lecture 3:
Special Topics
- Test Tools for DATA INTEGRITY
- Infrastructure Requirements
Lecture 4:
Change Control & SOPs
- Change Control
- SOPs
Want to register by P.O/Check?
We facilitate registration by P.O/Checks!Complete your registration in just a few easy steps
Please just download, fill out the registration form and send it to us either by email to support@globalcompliancepanel.com or just fax us at 302 288 6884.
Once the form is received, an invoice will be generated and sent back to your fax number.
Following this just send us your purchase order by fax at 302 288 6884
In case you wish to register by using check
NetZealous LLC,
DBA GlobalCompliancePanel,
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Suite 216, Fremont, CA 94539, USA
Phone: 1800 447 9407
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Group participations
Get fabulous discounts by participating in groups of two or more.| No | Attendees | Discount |
|---|---|---|
| 1 | 2 Attendees | 10% off |
| 2 | 3 to 6 Attendees | 20% off |
| 3 | 7 to 10 Attendees | 25% off |
| 4 | 10+ Attendees | 30% off |
To avail the above group discounts, all the participants should register by making a single payment
Call our representative TODAY on 1800 447 9407 to have your seats confirmed!
Angela Bazigos
CEO, Touchstone Technologies Silicon ValleySeasoned Executive with 40 years of experience in the Life Sciences & Healthcare Industries. Positions include Chief Compliance Officer http://morflearning.com/angelabazigos/. Experience combines Quality Assurance, Regulatory Compliance, Business Administration, Information Technology, Project Management, Clinical Lab Science, Turnarounds and Business Development. Past employers / clients include Roche, Novartis, Genentech & PriceWaterhouseCoopers. Co-authored & prototyped 21 CFR 11 guidance with FDA. Co-authored Computerized Systems in Clinical Research w/ FDA http://www1.diahome.org/~/media/4FA562336EBD46C58CDC43A8B7773095.ashx Patent on speeding up software compliance https://www.google.com/patents/US8266578. Recently quoted in Wall Street Journal for using training to bring regulatory compliance to the Boardroom http://blogs.wsj.com/riskandcompliance/2015/07/24/using-training-to-bring-compliance-to-boardrooms/ National Trainer for Society of Quality Assurance. Comments / collaborates with FDA on new guidance documents. Former President of Pacific Regional Chapter of Society of Quality Assurance. Stanford's Who's Who for LifeSciences: http://www.stanfordwhoswho.com/Angela.Bazigos.7144112.html#overview.