Services

  1. Regulatory 5/20/2011

    You need to find the most direct route to regulatory submission and regulatory approval for your bio pharmaceutical / biotech product or medical device so you can reach your market faster.

  2. Central Labs 5/20/2011
    You are facing increasingly complex global studies and clinical trials. What resources are available to help you overcome the challenges? Rely on our central laboratory services to deliver on the promise of quality, scientific expertise and proactive customer service according to your trial's needs.
  3. Model Based Drug Development 5/20/2011
    Turning healthy ideas into healthy humans has become a complex equation in the face of spiraling costs and rising scrutiny.
  4. Phase I/IIa 5/17/2011
    You need to safely advance your drug candidate through phase I/IIa. The key to achieving this objective — on time — is to focus on maximizing critical data through strategic study design.
  5. Quality Assurance

    Promoting excellence in clinical research
    At Rho, Quality Assurance (QA) is an independent group that promotes excellence by ensuring adherence to our processes, applicable regulations, and Good Clinical Practices (GCP). Our auditors’ focus on quality has been honed by years of multidisciplinary clinical research training, from extensive education on topics from software validation to GCP to FDA requirements.

  6. Medical Monitoring

    Addressing the clinical implications of research
    Rho’s Medical Monitors come from life science careers, including experience in medical and academic institutions. Our experts have both clinical and research experience, and some serve as academic investigators. They are able to apply their practical knowledge and experience to present solutions for the issues that occur in clinical trials and research studies.