Carolyn Troiano

ERP Project Manager, City of Richmond

Agenda

Part I The Keys to COTS Computer System Validation 1 hour

  • The Keys to COTS Computer System Validation
  • “GxP” Computer Systems
  • Regulatory Oversight
  • Software Categorization
  • “COTS” Software
  • “Cloud” Solutions
  • SaaS Solutions

Part II Step-Wise Process for COTS Risk-Based Computer System Validation and Change Control 1 hour

  • Computer System Validation (CSV)
  • System Development Life Cycle (SDLC) Methodology
  • Computer System Risk Assessment
  • CSV Policies and Procedures
  • System Operations and Maintenance
  • Organizational Readiness
  • CSV Documentation
  • System and Data Governance

Break 30 min

Part III 21 CFR Part 11 Compliance 1 hour.

  • FDA’s 21 CFR Part 11 Electronic Records and Electronic Signatures (ER/ES) Compliance
  • 21 CFR Part 11 Overview
  • 21 CFR Part 11 Compliance
  • Part IV Purchasing COTS Software 1 hour
  • Vendor Audit Background
  • Vendor Audit Strategy and Planning
  • Vendor Audit Execution
  • Validation Strategy
  • Validation Components

Part V Industry Best Practices 1 hour

  • FDA Inspection Trends
  • Industry Trends - Deficiencies
  • Industry Best Practices
  • Wrap-Up Session
  • Q&A 30 mins

Why should you attend

The attendee will learn how to comply with FDA's 21 CFR Part 11 guidance, which addresses the use of electronic records and electronic signatures (ER/ES). There are specific security and authentication requirements that are not necessarily covered by the standard computer system validation (CSV) approach, and go somewhat beyond this.

We will also address the roles of people involved in validating and supporting the systems, aside from just the standard system users. There are many tasks and functions they need to understand in order to be in compliance.

Who will benefit

Professionals in the following industries may also benefit from the content:

  • Pharmaceutical
  • Medical Diagnostics
  • Biotechnology
  • Tobacco and Related (Vapor, e-Cigarette, Cigar, etc.)
  • Animal Health
  • Any other FDA-regulated industry, plus any Life Science Consulting or Contracting firm
  • Information technology managers and analysts
  • Production managers and analysts
  • QC/QA managers and analysts
  • Clinical data managers and scientists
  • Compliance managers
  • Lab managers and staff
  • Automation analysts
  • Computer system validation specialists
  • GMP training specialists
  • Business stakeholders and individuals who are responsible for computer system validation planning, execution, reporting, compliance, training and audit
  • Consultants working in the life sciences, tobacco and related industries who are involved in computer system implementation, validation and compliance

Industries who can attend

This 180 -minute online course is intended for professionals in the Medical Device, Biotechnology,Pharmaceutical Industry. Although not presently stated in the draft , the same guide could be used by FDA Regulated Industries personnel.


Faculty Carolyn Troiano

Carolyn Troiano

Carolyn Troiano has more than 35 years of experience in computer system validation in the pharmaceutical, medical device, animal health, tobacco and other FDA-regulated industries. She is currently an independent consultant, advising companies on computer system validation and large-scale IT system implementation projects.

During her career, Carolyn collaborated with FDA and other industry representatives on 21 CFR Part 11, the FDA’s electronic record/electronic signature regulation.

Choose a Purchase Options


$299

Live Webinar - Single Participant

You get one log-in for the live 180-minute webinar for one participant, presentation materials and the opportunity to ask questions by phone and email

$489

Group Up to 5 Participants

You get 5 log-in for the live 180-minute webinar for all the participant, presentation materials and the opportunity to ask questions by phone and email


$389

Recorded Access Single User

You'll have access to one log-in for an archived recording of the entire 180-minute webinar, including the Q&A period, for 1 participant. You can log in any time of day or night. You'll also receive all presentation materials, plus an audio recording and transcript for the entire session. Delivery is approximately 48 hours after the session


$499

Training DVD

Within 48 hours delivered - Lifetime Access ,Audio recording of a webinar and reference manual delivered by download. Listen anytime on any compatible device.


$599

Live + Recorded Access

You get one log-in for the live & recorded 180-minute webinar for one participant, presentation materials and the opportunity to ask questions by phone and email