Connect with a procalcitonin clinical specialist

Get expert guidance to integrate procalcitonin (PCT) testing into your clinical protocols—improving patient outcomes and supporting antibiotic stewardship.

Procalcitonin (PCT) testing gives clinicians objective evidence of bacterial infection, helping reduce unnecessary antibiotic use and strengthen antibiotic stewardship. Connect with a PCT specialist below to discuss integrating it into your clinical and laboratory protocols.

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Expert support, tailored to your practice

Thermo Fisher Scientific, a leader in PCT innovation and BRAHMS biomarker development, provides specialized consultation to help you implement and optimize PCT testing. From protocol development to clinical adoption, our team helps you apply proven biomarker strategies with confidence.

Protocol design

Build PCT-guided antibiotic protocols tailored to your patient population—ICU, ED, post-surgical, or neonatal.

Results interpretation

Understand PCT kinetics, threshold values, and how to handle results that don't fit expected patterns.
 

Stewardship integration

Align PCT testing with your antibiotic stewardship program and CDC core elements for compliance.

Special populations

Considerations for neonates, immunocompromised patients, and post-surgical monitoring protocols.

Staff education

Resources to empower your team in PCT-driven decision-making.

Clinical support

Ongoing support from our clinical specialists for implementation questions and optimization.

Looking for technical support instead? Visit our technical reference library.

Trusted by leading institutions

  • 5,000+ hospitals worldwide using PCT-guided protocols
  • 4,000+ peer-reviewed publications supporting PCT use
  • FDA-cleared for antibiotic stewardship decisions (2017)
  • Backed by 30+ years of clinical evidence since the landmark 1993 discovery

Not ready to talk?

Download our PCT Implementation Checklist-a step-by-step guide to evaluating whether PCT fits your institution's needs. Or explore our Learning Center for clinical resources, webinars, and case studies.

Implementation checklist

A detailed overview of procalcitonin assay technology, clinical utility, and implementation considerations to support informed decision-making in laboratory and antimicrobial stewardship programs.

 

B·R·A·H·M·S Clinical Portal

The B·R·A·H·M·S Clinical Portal is your on-demand training platform for learning about procalcitonin (PCT) testing, from use in differential diagnosis and antibiotic treatment decisions to making bacterial co-infection assessments.
 

Clinical evidence library

Access peer-reviewed studies, clinical guidelines, and real-world evidence supporting the use of procalcitonin testing across infectious disease and antibiotic stewardship applications.

 

Frequently Asked Questions about PCT consultations

A PCT clinical specialist reviews your submission and contacts you within 2 business days via your preferred method. Initial consultations typically cover your clinical applications, current workflow, volume requirements, and any specific technical questions.

PCT Expert Consultation Service is Thermo Fisher Scientific's clinical support program connecting healthcare facilities with procalcitonin specialists. The service delivers tailored education, implementation guidance, order set development, and ongoing compliance assessment to help hospitals integrate PCT testing into antibiotic stewardship programs effectively.

Yes. During your consultation, you can request an on-site demo or arrange to visit a nearby reference site. We also offer virtual demonstrations for initial evaluations.

You'll be connected with a PCT clinical specialist-typically with a background in clinical chemistry, laboratory medicine, or molecular diagnostics who can address both technical and operational questions.

Healthcare facilities request PCT implementation support by contacting Thermo Fisher Scientific's clinical team. A Medical Science Liaison is assigned to guide your facility through protocol development, provide education on PCT kinetics and clinical applications, and assist with order set creation throughout the implementation process.

Most laboratories complete their evaluation in 4-8 weeks, including technical review, site assessment, and procurement discussions. Timelines vary based on your organization's approval processes.