Autoclave and Sterilizer Validation Services


Our deliverables provide you with properly documented evidence of your process meeting its acceptance criteria


Reports are provided within 2 Weeks upon receiving results and  completion of testing

Autoclave / Sterilizer Validation


Autoclave / Sterilizer Qualification and Validation Services

We specialize in providing the LifeSciences Industry with Autoclave and Sterilizer Validation Services. Additionally, we have expanded our customer base to include Sterile Compounding Pharmacies, Hospitals, the Dental Industry, and other organizations requiring compliance to the FDA and USP <797> requirements for validating sterile process and associated equipment. Our Validation Engineers and Microbiologists work closely with these organizations and deploy a scientific approach to customize a validation strategy that fits their specific and unique sterile process requirements.


  • Support Small & Large Scale Autoclaves and Sterilzers

  • Mulitple Load Pattern Testing

  • Glassware & Hardgoods Sterilization

  • Product Sterilization Validation


  • Off-The-Shelf Protocols

  • Customer Specific Protocol Writing

  • GxP Compliant Reporting

  • Temperature Uniformity Results

  • Chemical Indicator Results

  • Biological Indicator Results


  • Onsite and Offsite Support

  • Engineering Studies for Load Pattern Configuration

  • Cycle Developemnt Services

We will route your request quickly to the appropriate representative

Corporate Information

Quantus, Inc.

3 Valley Square

Suite 120

Blue Bell, PA 19422


MAIN: (866) 876-6537

FAX: (480) 247-4927

Quick Links

Our Services

CUSTOMERS remit Payments To:

QUANTUS, INC (#65043)

PO Box 4120

Portland, OR 97208

Mailing Addresses

SUPPLIERS send Bills To:

QUANTUS, INC (#23031)

PO Box 37635

Philadelphia, PA 19101-0635