In light of the pandemic situation events until September 2021 are cancelled. We will inform customers directly when the events are rescheduled.    
COVID CANCELLED: Project Management in Human Resources,   Boston MA, Jan 6-8, 2021
COVID CANCELLED: InterDrone, The International Drone Conference,   Cambridge MA, Jan 11-13, 2021
COVID CANCELLED: Supplier Management for Medical Device Manufacturers,   Cambridge MA, Feb 2-4, 2021
COVID CANCELLED: US Immigration Compliance Strategies,   Boston MA, Feb 15-18, 2021
COVID CANCELLED: Project Management Training,   Boston MA, Mar 3-5, 2021
COVID CANCELLED: Internal Audit, Fraud Risk Assessment Workshop,   Boston MA, Mar 22-25, 2021
COVID CANCELLED: Agile / Scrum Training,   Boston MA, Apr 12-14, 2021
COVID CANCELLED: Validation, Verification and Transfer of Analytical Methods,   Boston MA, Apr 19-21, 2021
COVID CANCELLED: Computer System Validation - Reduce Costs and Avoid 483s,   Boston MA, May 10-12, 2021
COVID CANCELLED: SharePoint Technology Conference,   Boston MA, May 26-28, 2021
COVID CANCELLED: Employment Laws Certificate Program,   Boston MA, Jun 7-9, 2021
Following events are tentatively planned but may be rescheduled, based on CDC guidelines or attendee registration interest .    
TENTATIVE: 21 CFR Part 11 Compliance,   Boston MA, Sep 22-24, 2021
TENTATIVE: Quality Control Laboratory Compliance,   Boston MA, Oct 6-8, 2021
TENTATIVE: Analytical Instrument Qualification and System Validation,   Boston MA, Nov 15-17, 2021
TENTATIVE: FDA's New Import Program for 2021,   Boston MA, Dec 7-9, 2021

Boston Professional Events List

3 hrs Virtual Seminar Computer System Validation

Oct 15, 2021 - 01:00 PM - Oct 16, 01:00 PM
WCS Consulting Inc.3190 Stirling Rd, Unit K4 ,Hollywood, FL 33021,

ZIP: 33021
Phone: 844-267-7299 | 954-947-5671  


This seminar will explore the best practices and strategic approach for evaluating computer systems used in the conduct of clinical trials and determining the level of compliance, based on validation and data integrity. We will walk through the entire System Development Life Cycle (SDLC) approach to validation of FDA-regulated computer systems, and will also discuss 21 CFR Part 11 and the importance of managing electronic records and signatures appropriately.

We will also walk through the entire set of essential clinical trial files that must be maintained before, during and after completion of the trial in the Trial Master File (TMF). This part of the discussion will also delve into the use of electronic Trial Master File (eTMF) systems and the pros and cons of doing so.

Finally, we will discuss what is needed to prepare for an FDA inspection of computer systems and data used in support of clinical trials. These are extremely valuable assets for any company doing this type of work, and best efforts are necessary to ensure data is maintained in a state of integrity throughout its lifecycle.

Sessioh Highlights

  • Learn how to identify “GxP” Systems

  • Discuss the Computer System Validation (CSV) approach based on FDA requirements

  • Learn about the System Development Life Cycle (SDLC) approach to validation

  • Discuss the best practices for documenting computer system validation efforts, including requirements, design, development, testing and operational maintenance procedures

  • Understand how to maintain a system in a validated state through the system’s entire life cycle

  • Learn how to assure the integrity of clinical data that supports trial work

  • Discuss the importance of “GxP” documentation that complies with FDA requirements

  • Learn about the policies and procedures needed to support your validation process and ongoing maintenance of your clinical trial systems in a validated state

  • Understand the key components of 21 CFR Part 11 compliance for electronic records and signatures

  • Know the regulatory influences that lead to FDA’s current thinking at any given time

  • Learn how to prepare the essential files for a Trial Master File

  • Understand how an electronic Trial Master File (eTMF) can improve trial management

  • Know the clinical data files that are essential to collect before, during and after the conduct of a trial

  • Learn how to best prepare for an FDA inspection or audit of a clinical trial related computer system


Lecture 1

“GxP” Systems
Computer System Validation (CSV)
CSV Maintenance
Lecture 2:

“GxP” Documentation Principles
Policies and Procedures
Lecture 3

21 CFR Part 11 Overview
21 CFR Part 11 Compliance
FDA Regulatory Compliance
Lecture 4

Computers and Data Integrity
Regulatory Influences
Industry Best Practices
Lecture 5

Clinical Trial Master File (TMF)
Electronic Trial Master File (eTMF)
Trial Master File Content
Before the Clinical Trial Begins
During the Clinical Trial
After the Clinical Trial

Lecture 6

Prepare for a Computer System Audit

Who will Benefit

This seminar is intended for those involved in clinical trial planning, execution and support, working in the FDA-regulated industries, including pharmaceutical, medical device, biological and tobacco. Functions that are applicable include research and development, manufacturing, Quality Control, distribution, clinical testing and management, clinical sample labeling, adverse events management and post-marketing surveillance.

You should attend this seminar if you are responsible for planning, executing or managing the implementation of any system governed by FDA regulations that is used to conduct, manage or support the conduct of clinical trials, or if you are maintaining or supporting such a system. Examples of who will benefit from this webinar include:

  • Clinical Data Analysts

  • Clinical Data Managers

  • Clinical Trial Sponsors

  • Information Technology Analysts

  • Information Technology Developers and Testers

  • QC/QA Managers and Analysts

  • Analytical Chemists

  • Compliance and Audit Managers

  • Laboratory Managers

  • Automation Analysts

  • Computer System Validation Specialists

  • GMP Training Specialists

  • Business Stakeholders/Subject Matter Experts

  • Business System/Application Testers

  • This seminar will also benefit any consultants working in the life sciences industry who are involved in computer system implementation, validation and compliance

Speaker Details

Speaker Profile

Carolyn Troiano has more than 35 years of experience in the tobacco, pharmaceutical, medical device and other FDA-regulated industries.

Wcs Seminars
Registration Details
(Contact us : 844-267-7299 | 954-947-5671  
Don't wait. Register TODAY or  Email  US [email protected]

Event Categories
Keywords: pharmaceutical


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