Trust Your Next In Vitro Study to SurePath DET™
Disinfectant Validation for Pharma, Biopharma, and Med Device
Disinfectant Validation for Pharma, Biopharma, and Med Device
“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.”
A SurePath DET in vitro study is the essential first step in establishing a robust contamination control program. Let us be your trusted partner.
Our team is deeply involved at every stage of the study:
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.
Our technical services team, comprised of industry-recognized scientists and engineers, provides exceptional expertise in contamination control strategies, process optimization, regulatory compliance, validation support and quality assurance. Navigate complex regulatory landscapes, reduce operational risks and accelerate your time-to-market with support from our professionals.
Meet the Team