Overview

webinar Based on GxP/GMP requirements, FDA requires that all computer systems that handle data regulated by FDA be validated in accordance with their guidance on computer systems. This is critical to develop the appropriate validation strategy and achieve the thoroughness required to prove that a system does what it purports to do. It also ensures that a system is maintained in a validated state throughout its entire life cycle, from conception through retirement. When used as intended, IT systems validation can provide increased process reliability, confidence, improved performance, and reduced operating expenses.

Why one should attend the training

Software validation is not just a regulatory necessity. It is fast becoming a necessity for the device industry's increasingly software-controlled environments.

Many companies struggle with understanding how to avoid major mistakes and inspection risk when validating software to FDA standards. This webinar will review the validation planning process with emphasis on avoiding common pitfalls. The attendee should leave the presentation confident in their ability to improve the level of validation success.

If data becomes invalid, based on improperly validating and maintaining the system that houses it in a validated state, the work related to the data would need to be repeated. This could result in a devastating loss to a company.

Learn how to develop the appropriate IT systems validation strategy. Understand how to effectively document the process of IT systems validation, and maintain current information about the various systems in your organization. We will discuss the key areas that are most important during inspection and audit, including security, data integrity, validation, training, and documentation.

Attendees will

  • Learn how to identify “GxP” Systems
  • Learn about the System Development Life Cycle (SDLC) approach to validation
  • Learn best practices for documenting IT 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 about the policies and procedures needed to support your validation process
  • Learn how to best prepare for an FDA inspection or audit
  • Lean clinical trial related IT systems validation


Webinar Takeaway

  • GxP/GMP Systems
  • FDA Regulatory Oversight over IT systems validation
  • Regulations: 21 CFR 11, Annex 11, GAMP 5
  • System Development Life Cycle (SDLC) approach to validation
  • Documenting IT Systems validation efforts
  • Policies and procedures needed to support the validation process
  • FDA audit preparedness as far as IT systems validation is concerned
  • Risk based approach to validation
  • Clinical trial related IT systems validation

key learning objectives

This webinar will focus on how to properly validate FDA regulated IT systems in order to ensure that security and data integrity objectives are met and FDA enforced compliance is met. We will discuss IT Systems Validation approach based on FDA requirements.

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, European equivalent Annex 11, GAMP 5 which deal with controlling risk and managing computer systems over their life cycle including validation. We will discuss what is needed to prepare for an FDA inspection of computer systems and data.

Who will Benefit

  • GxP/GMP Systems
  • IT Systems
  • IT Systems Validation
  • Data Management
  • Data Integrity
  • IT Systems Compliance
  • FDA Regulatory Oversight over IT systems validation

Industries who can attend

This 90-minute online course is intended for professionals in the Pharmaceutical, Clinical Data Management SaaS companies, and medical device companies . Although not presently stated in the draft , the same guide could be used by FDA Regulated Industries personnel

Faculty Eleonora Babayants


Galaxy Consulting Founder and President. She worked with quality assurance and compliance officers to develop and execute compliance has many years of GxP/GMP hands-on experience in regulated industries. strategies and programs. She participated in the implementation of compliance requirements.

Faculty Eleonora Babayants

Choose a Purchase Options

$289

Recorded Access Single - 6 month Access

You'll have access to one log-in for an archived recording of the entire 90-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

$399

MP3 Download (DVD)

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