Dermico was built on experience that only comes with time. Our scientific director Tim Houser, alongside consultants Dr. Gary Grove and Dr. Charles Zerweck, brings more than 40 years of hands-on clinical dermatology research to every project we take on. That experience shapes everything from how we approach a study design to how we interpret and present your results. Through our partnership with cyberDERM, inc., we also have immediate access to a full suite of advanced instrumentation from the world's leading manufacturers.
The same scientists who designed the methodology guiding your study from day one. Access to internationally recognized measurement methodologies. A complete instrumentation suite with no delays or sourcing gaps.
No two research challenges are the same, and we don't treat them that way. Through our partnership with cyberDERM, inc., we develop custom protocols, adapt existing instrumentation, and build specialized systems tailored to your product and goals. That flexibility matters most when you are working with a novel ingredient, an unconventional delivery format, or a claim that standard methodology was not designed to measure.
Custom protocol development for challenges other labs won't take on. Instrumentation adapted or purpose-built to your exact requirements. A research partner invested in your outcomes, not just your order.
Our skin measurement methodology produces reliable, objective data designed to meet the demands of regulatory review, clinical substantiation, and product development. We work to the same exacting standard on every study, so your results are defensible wherever they need to go. All client work is handled in strict confidence.
Objective, quantifiable results that accurately reflect what your product does. Findings structured to support regulatory submissions and marketing claims. Complete confidentiality on every project we handle.
From protocol design and subject recruitment through data analysis, statistical review, and reporting, we manage the full lifecycle of your study. QA and QC are embedded at every stage so nothing falls through the cracks and you always know where things stand.
One team, one relationship with no handoffs or coordination gaps Full FDA and ICH guideline compliance throughout Draft reports delivered promptly at study completion
