6 Most Common Problems in FDA Software Validation and Verification

6 Most Common Problems in FDA Software Validation and Verification
Product Code: : FDAQ-9281
Speaker : Carolyn Troiano
Date : 24th June 2019
Time : 11:30 AM PST | 02:30 PM EST
Duration : 90Min

Overview:

This webinar will help you understand in detail Computer System Validation (CSV) and how to apply the System Development Life Cycle (SDLC) Methodology when validating computer systems subject to FDA regulations.  This is critical in order 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.

We will discuss the phases within the SDLC, and how these form the basis for any CSV project.  The importance of the sequence of steps will also be covered.

Why Should You Attend:

  • Learn how to reduce the time and labor involved in a computer system validation effort by adequately planning your project
  • Learn how to leverage past validation efforts to optimize results
  • Learn how to ensure your team members are adequately trained to implement and maintain an FDA-regulated computer system in order to manage a successful outcome
  • Learn how efficient and effective testing can ensure that all deficiencies are captured before a system is put into production, allowing for a smooth go-live without delay
  • Learn how to keep on top of changes to the system over time to ensure it is maintained in a validated state and does not require a complete revalidation due to neglect
  • Learn how to manage organizational change at the outset of a new system implementation project in order to avoid sabotage and other attempts to resist new ways of conducting business
  • Learn how to evaluate business processes to ensure that these are optimized as the system is being developed and/or configured to enable improvements in efficiency and effectiveness of operations that will save money in the longer run
  • Learn how to document all validation work in order to ensure that revisits to the deliverables during subsequent system changes are efficient and do not require extra labor to dig through poorly documented information
  • Learn about potential pitfalls to the validation process through real industry examples
  • Learn how to avoid and/or mitigate potential pitfalls during the validation process

Areas Covered in the Session:

  • Computer System Validation (CSV)
  • System Development Life Cycle (SDLC) Methodology
  • Validation Planning
  • Risk Assessment
  • GAMP 5 System Categorization
  • Functional Requirements
  • IQ, OQ and PQ Testing
  • User Acceptance
  • Maintaining a System in a Validated State
  • Policies and Procedures
  • Training
  • Organizational Readiness
  • Documentation
  • Q&A

Who will Benefit:

  • Information Technology (IT) Analysts
  • IT Developers
  • IT Support Staff
  • QC/QA Managers and Analysts
  • Clinical Data Managers and Scientists
  • Compliance Managers and Auditors
  • Lab Managers and Analysts
  • Computer System Validation Specialists
  • GMP Training Specialists
  • Business Stakeholders using Computer Systems regulated by FDA
  • Regulatory Affairs Personnel
  • Consultants in the Life Sciences and Tobacco Industries
  • Interns working at the companies listed above
  • College students attending schools and studying computer system validation, regulatory affairs/matters (related to FDA) or any other discipline that involves adherence to FDA regulatory requirements

Speaker Profile:

Carolyn Troiano has more than 35 years of experience in the tobacco, pharmaceutical, medical device, and other FDA-regulated industries.   She has worked directly, or on a consulting basis, for many of the larger pharmaceutical and tobacco companies in the US and Europe, developing and executing compliance strategies and programs.


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