Sterilization, Packaging & Cleaning Validations


Validations are among the most crucial operational steps in the medical device path to market. Opportunities for missteps abound, so let Eagle guide you through the process with confidence, clarity and quickness. With our vast library of materials and experience with performing various validations for packaging, cleaning and sterilization, Eagle can keep your project on track for success.

What cannot be verified must be validated

While the conditions that require validation can sometimes be confusing, there need not be any concern about how to make that choice and with Eagle’s statistical know-how in Design of Experiments (DoE), a surefire program for reliable, repeatable process validation can be achieved. So, whether you’re unsure about verification or clear in the need for validation, or have special needs such as risk-based PFMEA driven validations, contact your Eagle Manufacturing Professional to investigate your options. Eagle can effectively assist with:

  • Sterility Assurance Validation
  • Packaging Validation
  • Sealing Equipment Validation
  • Cleaning Validation
  • Process Validation
  • Fixture/Assembly Validation