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Course Details

What is 21 CFR Compliance | 21 CFR Part 11 Regulations 2018


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DBA - Part Time
Birmingham City University
Birmingham City Business School

GlobalCompliancePanel
Regulatory and Compliance
Contact Provider
Boston,MA
TBC
Seminar
-
12
£935.70
Pharmaceuticals Biotech Medical Device Radiological Health Blood Products Companion Animals Food Cosmetics Tobacco Academia
WILL BE ANNOUNCED SOON, Boston,MA, 02128, Surrey, United Kingdom

 

Course "Validation and 21 CFR Part 11 Compliance of Computer Systems" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.

 

Overview:

 

Computer Systems Validation (CSV) also known as Software Validation is all-pervasive in the Life Sciences Industry. It is a requirement of all the predicate rules, as well as 21 CFR 11 and Annex 11. However, unless one knows how to implement CSV, it is often very hard to detect the requirement for CSV, and very hard to determine what needs to be done, to meet domestic and / or international regulations or business continuity requirements. In addition, the FDA has stepped up 21 CFR 11 inspections that include CSV.

This course will build on the Validation and 21 CFR 11 Compliance Basic Course, to give hands on experience on executing on the computer systems validation of a system, and to discuss related activities such as Validation Master Plan, Infrastructure Qualification, Project Management for Validation and Validation of Test Tools

 

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:

  1. Validation Master Plan
  2. Complete Validation for a System
  3. Excel Spreadsheet Validation
  4. Change Control
  5. SOPs
  6. Test Tools Validation
  7. Project Management for Validation

 

Who Should Attend:

 

  • VP of IT
  • Director of IT
  • Quality Managers
  • Project Managers (for CSV / 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

 

Industries:

 

  • Pharmaceuticals
  • Biotech
  • Medical Device
  • Radiological Health
  • Blood Products
  • Companion Animals
  • Food
  • Cosmetics
  • Tobacco
  • Academia

 

Agenda:

 

Day 1 Schedule

 

Lecture 1: 
Introduction/Background

  • Introductions / Participants' Understanding
  • Participants' Objectives for the Course (Please come prepared to discuss)

Lecture 2: 
Requirements at a High Level

  • Types of Requirements
  • Difference between User Requirements & Functional Requirements

Lecture 3: 
Detailed Requirements Study

  • Gathering Requirements
  • Entity Relationship Diagram
  • Process Decomposition
  • Risk Assessment for Requirements
  • Exercise on how to create Requirements

Lecture 4: 
Design

  • Design Specifications
  • Software Configuration and Build
  • Exercise on how to create Design Specifications

 

Day 2 Schedule

 

Lecture 5: 
CSV Detailed Study (Cont'd)

  • Traceability Matrix
  • Verification and Testing
  • Exercise Creating Validation Scripts
  • Exercise Creating Traceability Matrix

Lecture 6: 
Other Documents

  • Validation Plan
  • Test Protocols
    • Test Reports
  • Validation Report
  • Validation Registry

Lecture 7: 
Special Topics

  • Project Management for CSV
  • Infrastructure for CSV
  • Selecting software for 21 CFR 11 Compliance
  • Test Tools for CSV

Lecture 8: 
Change Control & Business Continuity

  • Change Control
  • Implementing Business Continuity for CSV

 

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: Boston, MADate:  March 1st & 2nd, 2018 and Time: 9:00 AM to 6:00 PM

Venue:  Four Points by Sheraton Boston Logan Airport Revere, MA   407 Squire Rd, Revere, Massachusetts 02151, United States

 

 Price:

Register now and save $200. (Early Bird)

Price: $1,295.00 (Seminar Fee for One Delegate)

Until January 20, Early Bird Price: $1,295.00 From January 21 to February 27, Regular Price: $1,495.00

Register for 5 attendees   Price: $3,885.00 $6,475.00 You Save: $2,590.00 (40%)*

Register for 10 attendees   Price: $7,122.00 $12,950.00 You Save: $5,828.00 (45%)*

 

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

[email protected]  

supp[email protected] 

Toll free: +1-800-447-9407

Phone: +1-510-584-9661

 Website: http://www.globalcompliancepanel.com

 

Registration Link - https://www.globalcompliancepanel.com/control/globalseminars/~product_id=901540SEMINAR?findcpd-March-2018-SEO

 

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

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