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Advanced Course: Validation & 21 CFR 11 Compliance of Computer Systems
Presented By Complianzworld
Thursday, November 20th at 9:00am EST - Friday, November 21st, 2014
Online sale ends: 11/20/14 at 8:00am EST
Complianz World
New York, NY 10036
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The Problem:

Computer Systems Validation (CSV) also known as Software Validation is all-pervasive in the Life Sciences Industry[1][2]. 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 attendees must have attended the Basic Validation & 21 CFR 11 Compliance. This is a very hands-on class and the attendees will be expected to use templates provided in the class to create the complete package for the validation of a system

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


Day One

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 Two

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


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


·         Pharmaceuticals

·         Biotech

·         Medical Device

·         Radiological Health

·         Blood Products

·         Companion Animals

·         Food

·         Cosmetics

·         Tobacco

·         Academia

[1] CSV = Computer Systems Validation. This term will be used to described both Computer Systems Validation and Software Validation

[2] Life Sciences industry includes all areas of Pharma, Biotech, Medical Devices, Food, Cosmetics, Companion Animals, Tobacco, Blood products etc.

Presented By

9:00am to 4:00pm
Doors open at 9:00am

General Admission: $799.00


Complianz World<br> New York, 10036


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