Xpertox Toxicology Services LLC

medical devices

About

OUR MAIN SERVICES Biocompatibility of Medical Devices According to EU MDR / US FDA Regulatory Requirements & ISO 10993 • Testing needs and assessment strategy • Chemical characterization of a device's components, device extractables and leachables • Biocompatibility/biological risk assessment • Final product evaluation Consulting in Toxicology • Data gap analysis and toxicological guidance • Toxicological risk evaluations and exposure assessments of raw materials and finished products • Searching and compiling toxicological information Systematic Literature Searches • Search strategy • Sources • List of keywords • Search process • Citation searching • Systematic review protocol

Technologies

Nginx Mobile Friendly WordPress.org Render Remote

Keywords

toxicological risk evaluations & exposure assessments biological evaluation of medical devices evaluation of toxicological studies toxicological consulting medical device safety evaluation compilation of toxicological informationdata extractables leachables biological evaluation toxicological information in vitro biocompatibility testing iso 10993 medical device chemical characterization regulatory biocompatibility extractables & leachables eu mdr biocompatibility biocompatibility consulting services preclinical safety assessment design & manage studies in toxicology for safety assessments reach biological safety biocompatibility testing for medical devices exposure assessment toxicological evaluation fda biocompatibility testing iso 109931 compliance toxicological risk assessment material characterization surface characterization

Location

Fribourg, Canton of Fribourg, Switzerland

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