Your event should be here ! To publish, manage, promote... To learn or to be formed ... Online registrations

Site language : English - Français
Ref : 26124
Event :Data Integrity, 21 CFR 11 & Annex 11 Implementation 2017

Dates :Thursday December 07th, 2017 - Friday December 08th, 2017

Location :Hilton San Francisco Airport Bayfront
600 Airport Blvd, Burlingame, CA 94010, USA
Sfo, Ca, United States

Type :Conference & Seminar - International audience

Accreditation :--


 

Further information

Course "Data Integrity, 21 CFR 11 & Annex 11 Implementation" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.

 

Overview:

 

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

 

Agenda:

 

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

 

Speaker

Angela Bazigos

CEO, Touchstone Technologies Silicon Valley

 

Seasoned 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.

 

Location: SFO, CA Date:  December 7th & 8th, 2017 and Time: 9:00 AM to 6:00 PM

Venue:  Hilton San Francisco Airport Bayfront   600 Airport Blvd, Burlingame, CA 94010, USA

 

 Price:

Price: $1,495.00 (Seminar Fee for One Delegate)

Register for 5 attendees   Price: $4,485.00 $7,475.00 You Save: $2,990.00 (40%)*

Register for 10 attendees   Price: $8,222.00 $14,950.00 You Save: $6,728.00 (45%)*

Register now and save $200. (Early Bird)

 

Sponsorship Program benefits for “Quality Assurance Auditing for FDA Regulated Industry” seminar

At this seminar, world-renowned FDA Regulated Industry subject matter experts interact with CXO’s of various designations. Executives who carry vast experience about FDA Regulated Industry and Experts get down to discussing industry-related best practices, regulatory updates, changes in technologies, and much more relating to FDA Regulated Industry.

As a sponsor of these seminars, you get the opportunity to have your product and company reach out to C-Level executives in FDA Regulatory -related industries and become known among these elite executives and subject matter experts. Apart from being seen prominently at these globally held seminars, you also get talked about frequently in our correspondences with our experts and these participants.

For More Information- https://www.globalcompliancepanel.com/control/sponsorship

 

Contact us today!

 

NetZealous LLC DBA GlobalCompliancePanel

john.robinson@globalcompliancepanel.com  

support@globalcompliancepanel.com

Toll free: +1-800-447-9407

Phone: +1-510-584-9661

 Website: http://www.globalcompliancepanel.com

 

Registration Link - http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901052SEMINAR?doctorama-December-2017-SEO

 

Follow us on LinkedIn: https://www.linkedin.com/company/globalcompliancepanel/

Like us our Facebook page: https://www.facebook.com/TrainingsAtGlobalCompliancePanel/

Follow us on Twitter: https://twitter.com/GCPanel

 

 

Location

Map and directions
Conference address :
Hilton San Francisco Airport Bayfront
600 Airport Blvd, Burlingame, CA 94010, USA
Sfo, Ca
United States
Map and directions

Further information

To access the information you need to be connected. Creating an account is easy and free!

Log to your account
Register on Doctorama

Announcer

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 [...]

Other events from GlobalCompliancePanel

Presentation sheet from GlobalCompliancePanel

Details

Data Integrity, 21 CFR 11 & Annex 11 Implementation 2017 Medicine - Pharmacy - Paramedic
data integrity, pharmaceutical data integrity, data management software, data management system, product data management, clinical data management, informatica data quality, data quality assurance
Everyone, 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
-- -- --
English

Other

For more information on Data Integrity, 21 CFR 11 & Annex 11 Implementation 2017, plsase contactr GlobalCompliancePanel

To display announcer website, obtain a letter of invitation, you must be logged

Log to my account
Register on Doctorama


Recommend this event