FDA Warning Letter - Consent Decree Software Validation

This FDA warning letter Webinar/training will discuss what to do to avoid additional software related compliance along with the response steps where the citations that directly or indirectly include automated system.

Why Should You Attend:

FDA inspectors are now being trained to evaluate software validation practices. Increasing use of automated manufacturing and quality systems have increased exposure. Most recalls can be traced back to computerized equipment, exposing the validation process to scrutiny. A third of recent warning letters included citations with respect to improper or ineffective validation.

Areas Covered in the seminar:

• Outline of FDA regulations as applied to software.
• Review of FDA software validation requirements.
• Review of FDA software expectations.
• Proactive steps to prevent additional software-related compliance and enforcement problems.
• Response steps where inspection citations directly or indirectly include automated systems.
• Forward planning.
• What to do about existing systems.
• The paradox of ongoing validation work.

Who will benefit:

This seminar will give valuable help to FDA regulated Pharmaceutical, Medical Device, Biotech, Diagnostics and Biological manufacturers who have received, expect or fear an FDA-483, Warning Letter or Consent Decree. The staff members who will benefit include:

• Internal auditors
• External auditors
• Remediation personnel
• Quality Assurance personnel and management
• SQA - Software Quality personnel
• Consultants
• Business managers responsible for system compliance
• IT / IS managers
• Regulatory affairs personnel and management
• Third-party certifier personnel