Nova specializes in GLP Testing, GLP Protocol Development, GLP Documentation, and GLP Reporting. Let Nova help you with  your next FDA or EPA submission.
Nova's Good Laboratory Practice (GLP) services are a custom quality system in which we plan, perform, monitor, record, archive and report your product's testing for submission to the FDA and or EPA.
Nova's FDA GLP studies include in vivo or in vitro experiments in which test articles are examined to obtain data on its properties and/or its safety, and are intended for submission to appropriate regulatory authorities.
Nova's most recent GLP Studies include:
| Medical Device Cleaning Validation |
Medical Device Disinfectant Validation |
Medical Device Sterilization Validation |
| Minimal Inhibitory Concentrations |
Disinfectant Efficacy |
DIS/TSS EPA Disinfectant Testing |
| AOAC Use Dilution Testing for Disinfectants |
AOAC Germicidal Spray Products |
AOAC Fungicidal Activity of Disinfectants |
| Virucidal Testing |
Antimicrobial Efficacy |
Cytotoxicity |
| Tuberculocidal Testing |
Radiopharmaceutical Testing |
Liquid and Chemical Sterilant Studies |
| High Level Disinfectant Studies |
Antibiotic Resistance Studies |
Antibiotic Potency |
| Bacteria Removal from Surfaces Studies |
Virus Removal from Surfaces Studies |
Fungus Removal from Surfaces Studies |
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