BioSiteHisto Laboratories provide compliant histopathological and in vitro laboratory services, which meet the requirements of OECD guidelines and regulatory compliance. We are aiming to develop flexible, long-term partnerships with our clients: all timelines are agreed in advance and regular liaison is maintained with Study Directors. We are experienced in multi-site studies and can provide specific documentation as required. Client QA inspections are always welcome. Our professional, highly educated and experienced team will offer excellent GLP laboratory services.
View our latest Statement of Good Laboratory Practice here.
Example of our GLP compliant services:
- Toxicity studies: Preclinical histopathology services including histological and immunohistochemical assays, analysis and interpretation of the slides.
- Medical device studies: Histolopathology studies of implantable materials and device. Our services include soft or hard tissue processing, histopathological assay analysis and interpretation of the slides, as well as comprehensive alternative in vitro testing methods, including cytotoxicity tests.
- In vitro testing and studies: Standardized, validated tests and assays to provide reliable data for regulatory purposes, including e.g. chemicals (REACH&CLP/GHS, biocides), products, cosmetics and biocompatibility of medical device.
We are also able to perform customized assays, tests and research for R&D customers. A wide range of cell lines, primary cells and 3D tissue models are in use for several end points. We also assist customers in developing test strategies to meet all specific needs for safety and efficacy.