At Ross Biotechnologies
We can more effectively accelerate your drug or medical device program by leveraging our unique expertise in executing programs from discovery to clinical trials, combined with our engineering, manufacturing, and regulatory capabilities.
Drug
Development
Our strong preclinical expertise in cell-free and cell-based analyses, ex vivo and in vivo analyses, murine animal models, and dissection and necropsy will simplify your program and help advance it more rapidly to clinical development.
Medical Device Development
From our long term experience with medical devices and combination products, we can help advance your device design through specifications, risk analysis, animal models, design verification and validation, manufacturing, human factors, and clinical all culminating into a Master Device File (MDF) for regulatory approval.
Regulatory Enabling Capabilities
With a combined experience of 40+ years enabling IND/IDE clinical trial approvals with the FDA, our team can help advance your drug or device into clinical development and improve your success in meeting primary efficacy and safety endpoints.