What Our Customers Say
- “The team at STERIS deftly managed the writing and execution of our study protocol, ensuring everything was on point.”
- “They communicated clearly up front about the materials needed, making the process smooth and hassle-free.”
- “The reports we received were clear and actionable, helping us implement an effective contamination control system.”
Why Choose STERIS SurePath DET?
- Proven Track Record: With decades of experience, we ensure your in vitro testing is done right the first time.
- Global Best Practices: Our approach leverages globally accepted test methods.
- Regulatory Standards Compliance: We test in conformance with applicable regulatory standards.
- Specialized Study Optimization: Our team understands the nuances of study design, optimizing each step for your custom requirements.
Contact STERIS today to learn how SurePath DET can put you on the right track toward compliance and efficiency.
Want to Learn More?
A SurePath DET in vitro study is the essential first step in establishing a robust contamination control program. Let us be your trusted partner.
The SurePath DET Advantage
- Efficient Process: We streamline each step, saving you time and resources.
- Scientifically Sound Studies: Our science-based approach ensures rigor and enables the best outcomes.
- Regulatory Compliance: We guide you through the ever-evolving compliance landscape, minimizing risks and ensuring a clear path to operational success.
Your First Step Toward a Validated Contamination Control Program
Our team is deeply involved at every stage of the study:
- Pre-Study Consultation: We collaborate with you to define study objectives and requirements.
- During the Study: Our team executes the testing process to ensure accuracy and reliability.
- Post-Study Support: We provide guidance on interpreting results and implementing your validated contamination control program.
Setting You Up for Validation Success
With years of in vitro study experience and the extensive resources of STERIS, our team can help you – no matter the project size. This allows you to focus on value-added activities that support quality, consistency and regulatory compliance for your organization.