Nonclinical Efficacy Testing » Non-Clinical CROs and Agencies » Cellomatics BioSciences Ltd.

Cellomatics BioSciences Ltd.

Cellomatics BioSciences Ltd. is a Nottingham-based preclinical-stage contract research organization (CRO) that provides support for drug development. In this article, we investigate and summarize the features of the company's contract non-clinical study services, the disease models it offers, and examples of non-clinical studies.

Cellomatics BioSciences Ltd.' Contract Nonclinical Trial Services Feature

Custom assay development to meet client needs

Cellomatics BioSciences Ltd,Develop assays (test methods) to help evaluate the efficacy of test compounds and provide customized servicesWe do this service. This service considers a variety of factors, including relevance, reproducibility, quality, interference, and cost,Customization to meet client needs and support from planning to completionI will do so.

We develop a variety of in vitro assays, primarily for biopharmaceutical and biotechnology companies. We provide the screening and evaluation needed at each stage of a drug development program.

A wide variety of facilities

To meet the diverse experimental needs of its clients, Cellomatics BioSciences Ltd. has installed a variety of equipment. The company has a powerful high-resolution imaging platform, theImageXpress® Pico Automated Cell Imaging Systemand high performance flow cytometer with user-friendly operation screen2020 Attune NxT Flow CytometerWe have also introduced a new system for the production of cellular biology. Through these investments, we are strengthening our technical capabilities to meet the needs of molecular cell biology.

Develop in vitro models with high predictive validity

Advanced in vitro experimental platform designed to reproduce human physiology, disease pathophysiology, and pharmacological responsesDevelopment of Translational Human Preclinical ModelsWe are currently working on a new series of models. These models encompass primary human cells, induced pluripotent stem cell-derived models, organoids, and 3D co-culture systems, and can provide higher predictive validity than traditional models.

Example of a pathological model owned by Cellomatics BioSciences Ltd.

INNOBEX, developed by Cellomatics BioSciences Ltd., is,Models designed to reproduce the complex structure and function of the human blood-brain barrier (BBB)It is. Using this model, drug compounds and their interactions within the BBB can be analyzed in detail. The company also uses primary human keratinocytes (keratinocytes) and freshly isolated immune cells,Also offers a model that faithfully reproduces the characteristics of psoriasisThe company is doing so.

Cellomatics BioSciences Ltd. Non-clinical Case Studies

No specific case studies were available on the official website.

Cellomatics BioSciences Ltd. Company Information

Cellomatics BioSciences Ltd. was founded in 2015. It provides preclinical in vitro bioassay services, specializing in therapeutic areas such as oncology, immuno-oncology, immunology and inflammation. The company evaluates the efficacy and safety of drugs to support research and development decisions.

Address10 Colwick Quays Business Park
Road No2, Colwick v Nottingham, Nottinghamshire, NG4 2JY, GB
Tel+44 (0)115 865 4101
Websitehttps://cellomaticsbio.com/

3 Recommended Contract Research Organizations
for Non-Clinical Studies
— by Target goal and Expertise

In non-clinical development, the choice of contract research organization shapes the quality of the data and the time it takes to reach the next decision. Below, three CROs are introduced by the type of study they support: pharmacology (efficacy) studies, safety studies, and pharmacokinetic (PK/PD) studies. Each summary describes the services the company offers so that you can match a provider to your target and development objective.

Pharmacology (Efficacy) StudiesDisease-Relevant Models for
Translational Drug Evaluation
SMC Laboratories, Inc.
Reference: SMC Laboratories, Inc. official website (https://www.smccro-lab.com/)

SMC Laboratories, Inc.

SMC Laboratories is a specialized non-clinical CRO focused on in vivo pharmacology and efficacy studies using disease-relevant animal models, particularly in fibrosis, inflammation, metabolic diseases, and oncology.

Areas of Expertise
Disease-Relevant Model Portfolio

SMC Laboratories offers models covering the liver, lung, kidney, intestine, and oncology. Its portfolio includes the proprietary STAM™ model for MASH, fibrosis, and hepatocellular carcinoma.

Study Design Based on Target Biology

Study plans are developed around the target biology, mechanism of action, disease stage, and development objective. Pharmacological endpoints can be combined with histopathology, biomarkers, and disease-specific readouts.

Support from Target Validation to Proof of Concept

With experience from more than 1,000 studies for clients in 30 countries, SMC Laboratories supports programs from target validation and candidate selection through in vivo proof-of-concept studies.

Safety StudiesComprehensive Safety Assessment for
Preclinical Development
Charles River Laboratories
Reference: Charles River Laboratories official website (https://www.criver.com/)

Charles River Laboratories

Charles River provides non-clinical toxicology and safety assessment services for programs ranging from exploratory safety studies to IND-enabling development.

Areas of Expertise
General Toxicology Across Study Designs

Services include single- and repeat-dose toxicology, dose-range finding, and general toxicology studies across multiple species and administration routes.

Non-GLP and GLP Study Support

Charles River supports both non-GLP and GLP studies, allowing sponsors to progress from early safety characterization to studies intended for regulatory submissions.

Integrated IND-Enabling Safety Assessment

Toxicology studies can be integrated with toxicokinetics, clinical pathology, histopathology, and safety pharmacology to support interpretation and IND-enabling safety packages.

Pharmacokinetic (PK/PD) StudiesConnecting Drug Exposure with
Pharmacological Response
Inotiv
Reference: Inotiv official website (https://www.inotiv.com/)

Inotiv

Inotiv provides integrated PK/PD, DMPK, and bioanalytical services to characterize drug exposure and its relationship with pharmacological response.

Areas of Expertise
Pharmacokinetic Characterization

PK studies characterize exposure, half-life, clearance, and other pharmacokinetic parameters needed to understand how a candidate behaves in the selected model.

Exposure–Response Evaluation

Pharmacokinetic data can be combined with pharmacodynamic endpoints and bioanalysis to evaluate the relationship between drug exposure and pharmacological response.

Integrated DMPK and Development Support

Integrated DMPK, pharmacology, and safety information supports candidate comparison, dose selection, dosing-frequency optimization, and decisions about subsequent preclinical development.

By Therapeutic Area
Disease Animal Models
and Reviews
Proven Capability, Expertise and Track Record
Top 3 Non-Clinical CRO Services