Contract Research Organization (CRO) Services

CellCarta is a leading global Contract Research Organization (CRO) and a dedicated scientific partner to the biopharmaceutical industry. We specialize in providing advanced, customized biomarker testing solutions designed to accelerate your therapeutic development pipeline. By partnering with our team of expert scientists, you gain access to integrated, state-of-the-art platforms and deep regulatory expertise, guiding your project seamlessly from discovery through all phases of clinical trials.  

Navigating the complexities of drug development requires a partner with comprehensive capabilities. CellCarta supports your program at every stage – from discovery to clinical development – with a suite of specialized laboratory services that generate robust, reliable data for key decisions and regulatory submissions. Our collaborative, science-first approach ensures that we function as a seamless extension of your team.  

Our strength lies in an integrated, multi-platform approach to biomarker science. We provide specialized CRO services across a range of cutting-edge technologies to address the unique challenges of your therapeutic area.  

• Biomarker Discovery & Validation CRO Services: Advance your precision medicine programs with our end-to-end biomarker solutions. We leverage deep expertise to support biomarker discovery, custom assay development, and full validation for exploratory and regulated trials, including development of companion diagnostics (CDx). Learn more about our Biomarker Development & Validation Services.  

• Histopathology & Pathology CRO Services: Our CAP/CLIA-certified histopathology laboratories provide comprehensive support for oncology and immunology research. We offer a full range of histology and pathology services – including advanced immunohistochemistry (IHC), immunofluorescence (IF), and AI-driven digital pathology – to deliver quantitative, actionable insights for your preclinical and clinical studies. Learn more about our Histopathology CRO Services.  

• Flow Cytometry CRO Services: Leverage our global flow cytometry platform for high-dimensional immune monitoring. Our immunology experts utilize all cytometry technologies to perform complex cell analyses in a GCLP-compliant environment, with assays standardized across all our global sites, leading to harmonized data generation. Learn more about our Flow Cytometry Services.  

• Genomic CRO Services: Unlock deeper biological insights with our advanced genomic platforms. From next-generation sequencing and digital PCR to single-cell sequencing, we provide comprehensive molecular profiling supported by customized data analysis essential for modern therapeutic development. Learn more about our Genomics offering. 

• Proteomic CRO Services: Our proven expertise in mass spectrometry allows us to support your large-scale proteomic analysis and biomarker quantification projects with sensitivity and accuracy. Explore our Mass Spectrometry Platform and what it can do for you.  

• Unparalleled Scientific Expertise: Our team is composed of experienced scientists with deep domain knowledge in fields such as immunology and oncology, but also in regulatory, ensuring the highest level of scientific rigor for your project.  

• Global Reach, Local Expertise: With nine state-of-the-art facilities across North America, Europe, Australia, and China, we deliver globally harmonized services while navigating local regulatory environments to support your international trials.  

• Integrated Technology Platforms: Access a comprehensive suite of technologies under one roof – spanning histopathology, proteomics, genomics, and immunology – for seamless data integration and faster turnaround times.  

• Quality & Regulatory Excellence: Our laboratories operate under the highest quality standards, including CAP accreditations/CLIA certifications and GCLP compliance, ensuring all data meet global regulatory requirements. 

Q: What is the role of a CRO in clinical trials?
A: In clinical trials, a CRO like CellCarta provides specialized laboratory services to support sponsors at every step. This includes developing and validating biomarker assays, processing and analyzing clinical samples, and generating the high-quality data required for regulatory submissions (e.g. FDA, EMA). By handling these scientific and analytical tasks, the CRO’s work helps determine a drug’s safety and efficacy, speeding up the path to approval.  

Q: How do I choose the right CRO partner?
A: Choosing the right CRO involves evaluating several factors. Look for scientific expertise in your therapeutic area, advanced technological capabilities (platforms and assays that fit your needs), a strong quality management and regulatory compliance record (CAP/CLIA, GCLP certifications), and proven experience with projects similar to yours. A strong CRO partner will also offer collaborative support, transparent communication, and a track record of success in helping clients reach their development milestones.  

Ready to accelerate your therapeutic development? Contact us.