GDR PHARMACEUTICALS
  • ㅤ
  • CRO Services
    • In Vitro Services
    • In Vivo Services
    • Animal Models
    • IND Enabling
  • Medical Device Services
    • Device Design
    • Medical Device File
    • Manufacturing
    • Clinical Development
    • Regulatory
  • Research
  • About Us
  • Contact Us
  • Partners
  • Careers
  • More
    • ㅤ
    • CRO Services
      • In Vitro Services
      • In Vivo Services
      • Animal Models
      • IND Enabling
    • Medical Device Services
      • Device Design
      • Medical Device File
      • Manufacturing
      • Clinical Development
      • Regulatory
    • Research
    • About Us
    • Contact Us
    • Partners
    • Careers
GDR PHARMACEUTICALS
  • ㅤ
  • CRO Services
    • In Vitro Services
    • In Vivo Services
    • Animal Models
    • IND Enabling
  • Medical Device Services
    • Device Design
    • Medical Device File
    • Manufacturing
    • Clinical Development
    • Regulatory
  • Research
  • About Us
  • Contact Us
  • Partners
  • Careers

We are an Expert Preclinical CRO specializing in advancing Drug and Medical Device developments.

Learn More About Ross Biotechnologies

We are an Expert Preclinical CRO specializing in advancing Drug and Medical Device developments.

Learn More About Ross Biotechnologies

At Ross Biotechnologies, accelerate your drug or medical device development program through our preclinical scientific expertises, engineering, and regulatory enabling capabilities.

Drug Development

Our strong preclinical expertises 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.   

Find Out More

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 allculminating into a Master Device File (MDF) for regulatory approval.

Find out more

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 and improve your success in meeting primary efficacy and safety endpoints.

Find out more

Ross Biotechnologies LLC

Copyright © 2026 Ross Biotechnologies LLC - All Rights Reserved.