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Selvita (Fidelta)

Selvita (Fidelta)A European CRO offering comprehensive support from drug discovery research to non-clinical developmentIt is. We offer contract research services including in vitro and in vivo pharmacology, DMPK, toxicology, and biomarker testing at our research facilities in Poland and Croatia, including the former Fidelta sites.

Features of Selvita's (Fidelta) preclinical contract research services

Evaluate candidate compounds in over 80 disease models

At Selvita,Over 80 validated rodent and rabbit modelsWe support in vivo pharmacological studies using . We cover a wide range of disease areas, including tumors, infectious diseases, inflammation, respiratory, digestive, fibrosis, metabolism, neurology, and immunology. Evaluations can be tailored to the development stage of candidate compounds, such as Proof-of-Concept, efficacy, PK/PD, Target Validation, and mechanism of action studies. In addition to existing models,Development of custom models tailored to the mechanism of action of compounds and research objectivesIt also supports this, allowing research plans to be developed even for candidate substances that are difficult to evaluate using standard testing systems.

non-clinical evaluation combining toxicity and pharmacokinetics

Integrating in vivo pharmacology, toxicology, histopathology, and DMPKis also a characteristic of Selvita's (Fidelta) preclinical studies. In toxicity studies, mice, rats, and rabbits are used to conduct single and repeat-dose toxicity, tolerability, maximum tolerated dose, and dose-ranging studies. Toxicity evaluations can combine toxicokinetics, clinical pathology, and histopathology. Because it is possible to evaluate not only drug efficacy, but also systemic effects and tissue-level changes after administration,If you would like to evaluate the efficacy and safety of candidate compounds in parallelcan also be used for. Please note that the official website currently offers toxicity servicesnon-GLPAs we are providing guidance as such, if a GLP toxicity study is required, individual confirmation is necessary.

Integrating PK/PD and biomarkers to support development

In in vivo PK,Pharmacokinetic studies using mice and ratsand conduct single and repeated dose studies, bioavailability, excretion, and tissue/CSF sampling. PK/PD data can also be combined with modeling and simulation. In addition, biomarker analysis utilizing qPCR, ELISA, flow cytometry, mass spectrometry, etc., is available.Multi-faceted evaluation of candidate compound effects by combining pharmacokinetic, pharmacodynamic, and biomarker dataYes, we can. We also offer bioanalytical services compliant with GLP/GMP, and our key feature is the ability to build a seamless research framework ranging from early-stage drug discovery research to developmental evaluations.

Source: Selvita official website
https://selvita.com/

An example of disease models owned by Selvita (Fidelta)

At Selvita,Models of inflammatory and respiratory diseases such as pulmonary fibrosis and asthmaWe support drug efficacy evaluations using . For example, in pulmonary fibrosis, non-invasive evaluation using Micro-CT is also possible. By combining image-based longitudinal observation with drug efficacy evaluation, changes in lung condition due to treatment can be continuously monitored. In addition to using existing models, we also accommodate the development of new models tailored to specific research objectives.

Nonclinical study cases of Selvita (Fidelta)

Search for lead compounds as candidate drugs for asthma

Fidelta, the predecessor of Selvita, from a major European pharmaceutical companyLead compound discovery targeting asthma, especially severe asthmaWe have a proven track record of being contracted for projects. Over a period of approximately 12 months, we conducted research combining medicinal chemistry, in vitro and in vivo pharmacology, DMPK, and pharmaceutical sciences, with a view toward future safety evaluation and candidate compound selection. By coordinating multiple specialized areas, this is an example of comprehensively supporting the process from the discovery of candidate compounds to the narrowing down of development candidates.

Source: Selvita official website Current report ESPI 33/2021
https://selvita.com/investors-media/reports/current/current-report-espi-33-2021

Company Information for Selvita (Fidelta)

Source: Selvita official website
https://selvita.com/
AddressPodole 79, 30-394 Kraków, Poland
Tel+48 12-300-5001
Websitehttps://selvita.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, Inc. official website (https://www.smccro-lab.com/jp/)
  • SMC Laboratories, Inc. 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, Inc. is an ideal partner for start-ups, biotech ventures, and academic institutions alike.
Safety Studies
Comprehensive Safety Evaluation for FIH Applications
Labcorp Holdings Inc.
(Labcorp Drug Development)
Labcorp Holdings Inc.
Reference: Labcorp Holdings Inc. official website (https://jp.labcorp.com/)
  • Labcorp Holdings Inc. 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 Holdings Inc.’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 Co., Ltd.
PhoenixBio Co., Ltd.
Source: PhoenixBio Co., Ltd. Official Website (https://phoenixbio.co.jp/)
  • PhoenixBio Co., Ltd.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 Co., Ltd. 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 Co., Ltd. delivers unmatched analytical precision and consistency.

By region
list of animal models
Expertise & Track Record
3 Recommended Contract Non-Clinical Testing Services