Medical Devices

BRF is expertise and routinely evaluating the medical devices Biocompatibility, Extractable & Leachable, Microbial Contamination under GLP & ISO 17025:2017 regulations according to the ISO 10993, US FDA, ASTM, USP and other standard guidelines.

Cytotoxicity Studies
Invitro Irritation Tests
Invivo Irritation Test
Systemic Toxicity Tests
Skin Sensitization Test
Pyrogenicity Test
Implantation Studies
Genotoxicity Testing
Microbiological Contamination Studies
Extractable & Leachable Studies
Other Toxicological Studies (Sub-acute, Sub-chronic, Chronic, Carcinogenicity, DART, Immunogenicity, Neurotoxicity).