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InnoSer

InnoSer is a preclinical contract research organization (CRO) with operations in Belgium and the Netherlands, specializing in rare disease and neurological disorder models.
This section outlines the key features of InnoSer’ preclinical services, representative disease models, and selected nonclinical study examples.

Features of InnoSer’ Contract Services for Non-Clinical Studies

Advanced Mouse Models Across a Broad Range of Disease Areas

InnoSer provides preclinical evaluations using an extensive portfolio of well-characterized and tightly controlled disease models,covering both common and rare disorders.Available models include neurological disease models for genetic disorders such as Fragile X syndrome, 22q11.2 deletion syndrome, and Angelman syndrome, as well as metabolic and cardiovascular disease models.
Comprehensive nonclinical services—combining behavioral assessments, pathological analyses, and PK/PD evaluations—enable detailed characterization of disease-specific effects and pharmacological mechanisms.
All models are precisely designed and maintained to closely reflect human disease pathology with high translational relevance, making them well suited for efficacy and mechanism-of-action studies of drug candidates.

High Standards of Animal Welfare and Quality Control Through AAALAC Accreditation

Preclinical studies are conducted at European animal research facilitiesaccredited by AAALAC International (Association for Assessment and Accreditation of Laboratory Animal Care International),ensuring compliance with globally recognized standards for animal welfare and care. AAALAC accreditation represents an independent validation that animal use is conducted ethically and scientifically, supported by standardized husbandry, health monitoring, and stress-reduction protocols.
In addition, InnoSer holds ISO 9001 certification for quality management systems, ensuring transparency, reproducibility, and regulatory compliance across all research processes.
This robust infrastructure supports the generation of reliable data suitable for regulatory submissions, including IND-enabling study packages.

Integrated Preclinical Study Design and Customized Support

InnoSer’ preclinical services extend beyond model provision to offerintegrated support from early discovery through IND-enabling safety evaluations.Study designs are tailored to each stage of the drug development pipeline, combining pharmacokinetics (PK), toxicology, efficacy studies, pathological evaluation, and biodistribution analyses as required.
The company also supports integrated in vitro and in vivo study designs and offers customized model adaptations and analytical approaches to meet project-specific requirements of pharmaceutical companies and research institutions.
This flexible and integrated framework enables high-precision evaluation of drug efficacy and safety, facilitating efficient progression toward human clinical trials.

Examples of Disease Models Available at InnoSer

The Fmr1 knockout (KO) mouse model developed by InnoSer is a highly translational preclinical model thatrecapitulates key pathological features of human Fragile X syndrome (FXS).
FXS is caused by mutations in the FMR1 gene and is associated with cognitive impairment and autism spectrum disorders. Established on C57BL/6J and FVB genetic backgrounds, this model exhibits altered spontaneous behavior, cognitive deficits, hyperactivity, and reduced social interaction.
Clinically relevant biomarkers, including electrophysiological endpoints such as cortical evoked potentials, can also be assessed, supporting the evaluation of therapeutic candidates.

InnoSer also offers Alzheimer’s disease (AD) models, including multiple transgenic mouse models thatreproduce hallmark AD pathologies such as amyloid plaque formation and tau pathology.These include APP transgenic models, transgenic tau models, and tau seeding models that exhibit abnormal tau accumulation.
The models are designed to assess AD-related phenotypes including neurodegeneration, neuroinflammation, and cognitive and behavioral impairments, and are suitable for evaluating diverse therapeutic approaches such as small molecules, antibody-based therapies, and gene therapies.

InnoSer Non-Clinical Case Study

Efficacy Evaluation Using an Acute Psoriasis-like Skin Inflammation Model

InnoSer has conducted efficacy studies using an IL-23–induced acute skin inflammation model of psoriasis. In this model, intradermal injection of the pro-inflammatory cytokine IL-23 into the mouse ear rapidly induces psoriasis-like features, including increased ear thickness, inflammatory cell infiltration, and epidermal hyperplasia.
The model recapitulates key inflammatory pathways observed in human psoriasis and is well suited for early in vivo evaluation of anti-psoriatic drug candidates. Quantitative assessment of ear swelling and digital pathology analyses demonstrated that the evaluated therapeutic agent exhibited statistically significant efficacy in this IL-23–induced psoriasis model.

InnoSer Company Information

Address Agoralaan A bis, 3590 Diepenbeek, Belgium
Tel +32 (0) 11 14 07 68
Website https://www.innoserlaboratories.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