FUJIFILM Wako Pure Chemical Corporation is a provider of GLP-compliant safety studies based in Medford, with extensive experience in non-clinical testing. This section introduces the company’s features in non-clinical studies, examples of disease models, and case studies. We hope you can use this information as a reference when selecting a reliable partner for your non-clinical studies.
FUJIFILM Wako Pure Chemical Corporation provides pharmacological efficacy studies covering a broad spectrum of disease areas, including the neurology, cardiovascular, metabolic, and respiratory, digestive system, renal and urinary systems, allergy, inflammation, immune systems, and immuno oncology. The company also offers in vitro Magnus assays to accommodate diverse testing needs for different drug development stages. They are GLP compliant; offering comprehensive support throughout early discovery to later drug development.
FUJIFILM Wako Pure Chemical Corporation has established a robust platform for pharmacokinetic (PK) studies with Good Laboratory Practice (GLP) and reliability standards. They offer in vivo study for absorption, distribution, metabolism, and excretion (ADME) of drug candidates. They thrive to deliver precise pharmacokinetic data to support each stage of drug development and ensure smooth transition to clinical stage.
The company also provide high-quality safety /toxicity study and mutagenicity study. You can determine initial human doses and safe dose ranges by clarifying target organs, dose dependency, exposure relationships, and recovery potential. Leveraging analytical and bio-related technologies cultivated over many years, they offer in vivo study and a wide range of analytical service.
Kamakura Techno-Science is a contract research organization who provides safety and pharmacological evaluations. They utilize bio-related technologies developed in Toray’s life science business. The company conducts a wide variety of studies in neurological, cardiovascular, metabolic, respiratory, gastrointestinal, renal/urinary, and allergic, inflammatory,and autoimmune related.
Fukushima Cell Factory offers research support services for drug development by utilizing technologies and expertise cultivated through the Fukushima Pharmaceutical Industry Support Project. Services include cell and specimen storage, cell culture, cell characterization, and cell sorting.
Fukushima Pharmaceutical Industry has developed Tumor-bearing animal model that maintains original tumor’s histopathology and gene expression characteristics. This model is suited for evaluating immuno-oncology indications by transplanting the PDX into immunodeficient mice. Ex vivo testing is also available without transplantation, enabling direct evaluation of drug efficacy.
This model is induced by cerebral ischemia with middle cerebral artery occlusion and bilateral common carotid artery ligation. Rats are used, and reports are typically delivered within one month.
FUJIFILM Wako Pure Chemical Corporation offers a wide range of development support services, including drug discovery, regenerative medicine, and gene therapy.
| Address | 3-1-2 Dosho-machi, Chuo-ku, Osaka, Japan |
|---|---|
| Tel | 06-6203-3741 |
| Website | https://www.fujifilm.com/ffwk/ja |
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.
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.
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 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.
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.
Charles River provides non-clinical toxicology and safety assessment services for programs ranging from exploratory safety studies to IND-enabling development.
Services include single- and repeat-dose toxicology, dose-range finding, and general toxicology studies across multiple species and administration routes.
Charles River supports both non-GLP and GLP studies, allowing sponsors to progress from early safety characterization to studies intended for regulatory submissions.
Toxicology studies can be integrated with toxicokinetics, clinical pathology, histopathology, and safety pharmacology to support interpretation and IND-enabling safety packages.
Inotiv provides integrated PK/PD, DMPK, and bioanalytical services to characterize drug exposure and its relationship with pharmacological response.
PK studies characterize exposure, half-life, clearance, and other pharmacokinetic parameters needed to understand how a candidate behaves in the selected model.
Pharmacokinetic data can be combined with pharmacodynamic endpoints and bioanalysis to evaluate the relationship between drug exposure and pharmacological response.
Integrated DMPK, pharmacology, and safety information supports candidate comparison, dose selection, dosing-frequency optimization, and decisions about subsequent preclinical development.