Data Without Integrity Is Just Numbers: Data Integrity & Record (Arlington, VA, United States - July 12-13, 2018)

  • ID: 4535711
  • Conference
  • Location: Arlington, VA, United States
  • 2 Days
  • NetZealous LLC
  • Conference Dates: July 12-13, 2018
1 of 4

Course "Data Without Integrity Is Just Numbers: Data Integrity & Records" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.

The impact of Data Integrity issues on a regulated company can be significant: it can result in recalls of products, warning or untitled letters, import alerts, injunctions, seizures, legal action, etc. These regulatory actions can have significant financial impact to the company. However, and most importantly, Data Integrity issues can lead to potential patient harm!!

Defined by the Medicines and Healthcare Products Regulatory Agency (MHRA) as "the extent which all data are complete, consistent and accurate throughout the data lifecycle", Data Integrity is increasingly the focus of regulatory agencies round the world.

Companies must now ensure that they are appropriately addressing Data Integrity and data integrity. This includes organizational, procedural and technical controls that must be considered as part of an overarching data integrity system. In addition, the effort and resources committed to Data Integrity must be commensurate with the role it plays in assuring product quality.

To ensure Data Integrity, a GxP regulated company needs to abide by principles, current regulations and industry best practices on the expectations for the management GxP regulated records and data. These principles, regulations and best practices, ensure that data is complete, consistent, accurate, secure and available throughout the record life cycle. This approach is intended to encourage innovation and technological advances while avoiding unacceptable risk to product quality, patient safety and public health.

Key implementation considerations for a corporate Data Integrity program, include development of a high-level strategy, identifying and gaining executive sponsorship, focusing on management accountability, implementing tools for knowledge sharing and developing and providing the appropriate levels of training. An effective Data Integrity program includes addressing of behavioral factors and drives a strategy that focuses on prevention, detection, response and continuous improvement.

The Seminar:

This Seminar addresses the integrity of GxP records and data used within the regulated industries including pharmaceutical, biological, medical devices, cosmetics, food and any other industry where Data Integrity is important. It provides a method for managing risk to record and Data Integrity.

Learning Objectives for the seminar include:

  • Data Integrity Requirements
  • Critical Areas of Regulatory Focus and Concern
  • Key Concepts
  • A Framework for Data Integrity and Human Factors
  • A Complete Data Life Cycle Approach as Part of a Quality Management System, from Creation to Destruction
  • How to Apply Risk Management to Data Integrity

Why you 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
  • Regulators
  • Vendors
  • Suppliers
  • Outsource Service Providers


  • Pharmaceuticals
  • Biotech
  • Medical Device
  • Radiological Health
  • Blood Products
  • Companion Animals
  • Food
  • Cosmetics
  • Tobacco
  • Academia
Note: Product cover images may vary from those shown
2 of 4

Day 1 Schedule

Lecture 1:
Introduction and Background
Introductions / Participants' Understanding / Participants' Objectives for the Course (Please come prepared to discuss)
Regulatory Focus
Data Integrity Requirements

Lecture 2:
Data Integrity Framework
Elements of the Data Integrity Framework
Human Factors in Data Integrity
Data Integrity Maturity Model

Lecture 3:
Quality Risk Management
Process Risk Management
Quality Risk Management
Product and Process Context

Lecture 4:
Data Life Cycle
Data Creation
Data Processing
Data Review, Reporting and Use
Data Retention & Retrieval
Data Destruction
Integrating Data Integrity into Existing Records Management Process

Day 2 Schedule

Lecture 5:
Data Integrity Management
Corporate Data Integrity Program
Data Integrity Maturity Model
Human Factors
Inspection Readiness

Lecture 6:
Auditing & Audit Trails
Data Audit Trail
Audit Trail Review
Data Auditing
Periodic Review

Lecture 7:
Data Integrity for Electronic Records / Electronic Signatures (ERES)
User Requirements
Process Mapping & Interfaces
Controls for Electronic Records / Electronic Signatures
Data Integrity for Spreadsheets & End-User Applications
Data Integrity for IT Infrastructure

Lecture 8:
Data Conversions
Retention, Archiving & Migration
Paper Records & Hybrid Situations
Converting Electronic to Alternative Format or Alternative Format Hybrids
Quiz: Jeopardy!!!!
Data Integrity

Note: Product cover images may vary from those shown
3 of 4


4 of 4
  • Angela Bazigos Ms Angela Bazigos,
    CEO ,
    Touchstone Technologies Silicon Valley

    Angela Bazigos.CEO of Touchstone Technologies Inc. She has 40 years of experience in the Life Sciences & Healthcare Industries. Experience combines Quality Assurance, Regulatory Compliance, Business Administration, Information Technology, Project Management, Clinical Lab Science, Microbiology, Food Safety, Turnarounds and Business Development. Past employers / clients include Roche, Novartis, Genentech & PriceWaterhouseCoopers. Positions include Chief Compliance Officer at Morf Media. Co-authored & prototyped 21 CFR 11 guidance with FDA. Co-authored Computerized Systems in Clinical Research w/ FDA. Patent on speeding up software compliance. Recently quoted in Wall Street Journal for using training to bring regulatory compliance to the Boardroom. 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 Life Sciences.

Note: Product cover images may vary from those shown
5 of 4


Courtyard Arlington Crystal City/Reagan National Airport
2899 Jefferson Davis Highway
Arlington, VA
United States

Note: Product cover images may vary from those shown