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Sterility Validation 101:
Ensuring a robust sterilization
validation program from start to finish


View our on-demand webinar to learn the many factors to consider when developing and registering a sterile product to ensure your product sterilization process is properly validated and documented, including:
  • Applicable FDA and international regulations/guidance
  • Terminal sterilization vs. Aseptic processing
  • The right sterilization method for the right materials
  • The impact of your manufacturing environment and processes
  • Packaging considerations
  • Sterilization validation and ongoing maintenance sterility testing
  • Preparing for an audit
  • Current FDA views on sterilization and the impact to your 510K
Please register below to join our
mailing list & access our
on-demand session.