Process Validation Online Event

Event Details
  • Days
    Hours
    Min
    Sec
  • Start Date
    13 May 2026 13:00
  • End Date
    13 May 2026 18:00
  • Door Time
    12:55
  • Status
    Upcoming
  • Location
Principal Process Validation Consultant
ValSource Inc.

The webinar will provide a practical overview of validation across the full process lifecycle, from process design and qualification through continued process verification. Key topics include process characterization and the data-driven identification of critical quality attributes and critical process parameters, as well as the definition and implementation of a robust control strategy integrating process, equipment, sanitization controls, and advanced data analytics. The program will also address the use of AI-supported tools for trend analysis, anomaly detection, and enhanced process understanding, alongside sanitization validation and data requirements to demonstrate effective microbial control under worst-case conditions. The session will conclude with continued process verification and trending to ensure the process remains validated during routine manufacturing.

Webinar focus areas:

  • Validation of the process lifecycle covering design, qualification, and ongoing verification.
  • Process characterization and data-driven identification of critical quality attributes and process parameters.
  • Definition and implementation of a robust control strategy for process, equipment, and sanitization.
  • Use of AI and advanced analytics to support process understanding, trend evaluation, and early risk detection
  • Validation of sanitization and data support for effective microbial control under worst-case conditions.
  • Continued process verification and trending to confirm the process remains validated.

    Who Should Attend:

    Quality Assurance and Quality Systems professionals
    Manufacturing and Operations staff
    MS&T / Process Development and Process Engineering teams
    Validation, Qualification, and Technical Services personnel
    Microbiology and Environmental Monitoring teams
    Regulatory Affairs and Compliance professionals
    Site leadership responsible for GMP readiness and inspections

  • 199
    Full Access
  • Full online access
  • Post-event documentation
  • Certificate of attendance
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    Event Details
    • Days
      Hours
      Min
      Sec
    • Start Date
      13 May 2026 13:00
    • End Date
      13 May 2026 18:00
    • Door Time
      12:55
    • Status
      Upcoming
    • Location