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Certis Oncology Solutions

Certis Oncology Solutions is a non-clinical CRO that undertakes research and development for pharmaceutical and biotechnology companies. Here we survey and summarize the characteristics of the company's contract services in non-clinical studies, the pathological models it possesses, and examples of non-clinical studies.

Certis Oncology Solutions' Contract Non-clinical Trial Services Feature

Received CLIA certification

Certis Oncology Solutions is CLIA certified, a law enacted in the United States in 1988 to ensure the quality of clinical laboratories. Today, all clinical laboratories that provide laboratory services in and for the United States are required to obtain this certification.

Provides a unique platform

Certis Oncology Solution is a life science technology company,Realization of precision medicine in cancer treatmentOur goal is to provide the best possible clinical translatability. In this context, we offer a unique platform, Certis Oncology Intelligence®, that addresses the clinical translatability issues of traditional non-clinical models. models to support developers in making more accurate decisions.

Develop models for various clinical scenarios

With advances in cancer treatment, preclinical drug development is becoming more personalized and customized, making it important to select a model that can accurately reflect the objectives of the clinical trial.

In this situation, the use of custom-made cancer models for specific purposes makes the decision to continue development easier and reduces the time and effort required to search for a vast number of models. The company to address a variety of clinical scenarios, including radiation therapy, a commonly used cancer treatment worldwide,Develop custom in vitro and in vivo modelsThe company is doing so.

An example of a pathological model owned by Certis Oncology Solutions

The company has orthotopic PDX (O-PDX) models for a wide range of cancer types, including brain (GBM), breast, pancreas, lung, and sarcoma. For example, the company has expertise in surgical transplantation of HER2+ breast cancer cell lines into the brain and custom development of metastasis models that exactly replicate the metastasis from breast cancer to the brain observed in clinical practice. Thus, the company has developed brain stereotactic transplant metastasis models of HER2+ breast cancer and KRAS pathway targetingStrengths in developing custom models for drug evaluationWe have a

Certis Oncology Solutions' Non-clinical Case Studies

Evaluating therapeutic effects on tumor models

A case study on an efficacy trial evaluating the efficacy of a treatment on a specific tumor model is presented. In this example, an O-PDX model of a patient's tumor diagnosed as a muscularis species (RMS) was used to test a combination of 10 different therapeutic agents for 4 weeks in a tumor model implanted in immunocompromised mice. Results,Tumor shrinkage with 6 different treatment methodsThe most effective treatment achieved a 96.5% tumor reduction. In contrast, the no-treatment group experienced a seven-fold increase in tumor size.

Reference: Certis Oncology Solutions official website (https://www.certisoncology.com/clinical-results/orthotopic-pdx-pharmacology-study/)

Certis Oncology Solutions Company Information

Founded in 2016, Certis Oncology Solutions is a life science technology company whose mission is to enable precision medicine in cancer treatment. To provide compelling evidence of treatment effectiveness, the company offers a proprietary platform, Certis Oncology Intelligence®.

Address5626 Oberlin Drive, Suite 110, San Diego, CA 92121, United States
Tel858-952-1820
Websitehttps://certisoncology.com/
3 Recommended Contract Research Organizations for Non-Clinical Studies
— by Target goal and Expertise

In drug discovery, the quality and efficiency of non-clinical studies have a direct impact on clinical success rates, development costs, and overall length of time required in R&D. In recent years, there has been more demand for clinically relevant data, globally accepted reliability, and accurate early-stage screening. Thus, it is more important than ever to select the right CRO (Contract Research Organization) for strategic approach.
In this article, we highlight three CROs with proven technical capabilities, expertise, and long standing track records. These are our TOP 3 choices based on their capabilities and the specific target goals of the researchers for their non-clinical studies.

Pharmacology (Efficacy) Studies
Replicate unknown pathological models and
Discovery to clinically oriented drug evaluation
SMC Laboratories, Inc.
SMC Laboratories, Inc.
Reference: SMC Laboratories official website (https://www.smccro-lab.com/jp/)
  • SMC Laboratories has established a disease models using patented mouse technologies. The company has established proprietary pathological models—particularly in liver disease and fibrosis—and continues to expand their approach across a wide range of models in cancer, inflammation, and metabolic diseases.
  • From exploratory research to clinically oriented efficacy evaluation, SMC offers customized study designs, dosing strategies, and evaluation analysis tailored to each project. Their collaborative approachallows researchers to discuss and refine study plans together with SMC’s expert scientists.

  • With flexible small-scale study options and strong technical support, SMC Laboratories is an ideal partner for start-ups, biotech ventures, and academic institutions alike.
Safety Studies
Comprehensive Safety Evaluation for FIH Applications
labcorp
(Labcorp Drug Development)
labcorp
Reference: labcorp official website (https://jp.labcorp.com/)
  • labcorp provides a fully integrated GLP testing system aligned with international regulatory standards, including FDA, EMA, and PMDA requirements. All studies are conducted under ICH-compliant quality assurance, making it ready for data submission.
  • The company has extensive expertise in long-term toxicity studies such as Segment I–III reproductive and carcinogenicity studies, as well as 2-year chronic toxicity assessments.
  • labcorp’s comprehensive approach enables sponsors to efficiently outsource the entire preclinical package from toxicology, toxicokinetic (TK), and safety pharmacology study design to execution. This accelerates a path to First-in-Human (FIH) trials. For most of the global drug developers, this all-in-one service structure minimizes cost, risk, and expedite the time before advancing to clinical phase.
Pharmacokinetic (PK/PD) Studies
High-Precision Bioanalysis for Clinically Predictive PK/PD Evaluation
PhoenixBio
PhoenixBio
Source: PhoenixBio Official Website (https://phoenixbio.co.jp/)
  • PhoenixBio offers pharmacokinetic and hepatic metabolism studies using their proprietary PXB-mouse®, a humanized-liver chimeric mouse model. This platform enables the acquisition of data with high clinical correlation in ADME, drug–to-drug interaction studies, bridging the gap between preclinical and clinical stages.
  • With advanced LC-MS/MS-based bioanalysis, PhoenixBio provides aseamless workflow from plasma concentration measurement and metabolite identification to quantitative validation.

  • The company offersan integrated evaluation analysiscovering pharmacokinetics, hepatotoxicity, and safety with flexibility to accommodate complex modalities such as oligonucleotide and middle-molecule therapeutics. For compounds where hepatic metabolism is a development bottleneck—or where quantitative, reproducible exposure data are critical—PhoenixBio delivers unmatched analytical precision and consistency.

Consult Phoenix Bio for PK/PD analysis with a clinical focus
By region
list of animal models
Expertise & Track Record
3 Recommended CRO for Non-Clinical Studies