Partnering Solutions
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Project Management
6/14/2011
For 25 years, Rho has benefited clients from pharmaceutical, biotechnology, and federal research institutions by successfully leading their clinical research projects from initiation to closure.
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Quality Assurance
6/14/2011
At Rho, Quality Assurance (QA) is an independent group that promotes excellence by ensuring adherence to our processes. Our auditors' focus on quality has been honed by years of multidisciplinary clinical research training, from extensive education on topics from software validation to Good Clinical Practices (GCP) to FDA requirements and processes.
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Data Standards
6/14/2011
Data Standards is one of Rho's strongest capabilities and one of the services most in demand by our clients. Our company's distinct advantage is our knowledge of the standards and the tools we have developed to support their use.
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Hematology Oncology Brochure
12/26/2018
Trial design, site selection and recruitment, all tailored to the specific oncology indication. It’s what we do. Best.
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Rescue Services
6/14/2011
Due to the complexity of clinical trials and the constant struggle to keep trials on schedule, Rho is often called on to resolve issues when processes don't go as planned.
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Patient Access & Engagement Services
4/8/2019
UBC helps pharmaceutical and biotech manufactures overcome access and adherence challenges by using the right combination of our high-touch services and high-tech solutions. Our patient support programs are powered by UBC Pathways™, our proprietary suite of healthcare analytics and technology solutions.
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Comprehensive Primary Packaging Brochure
5/3/2019
From sourcing materials to designing sustainable structures to protect and preserve the shelf life of your product, our experts incorporate Package Smart™ solutions to bring your product to market.
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Post Approval Studies
6/14/2011
Whether you’re working to provide new treatment options through label extensions or trying to demonstrate efficacy over other marketed medications, Rho has the research power that will advance your Phase IV clinical trials.
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Clinical Manufacturing
10/28/2019
PCI offers a broad range of services to address the manufacturing needs of our clients at each stage of the product lifecycle. Central to PCI’s international service offering is our capability to manufacture a range of dosage forms in compliance with current GMP standards.
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Real World Evidence
5/10/2019
Implementing an enterprise-wide Real World Evidence strategy is essential to meet the growing demands of regulators, patients, healthcare providers and payers to support approval, treatment decisions and reimbursement. Fluency in evidence-generation combined with operational expertise in RWE are crucial for capitalizing on the potential RWE has to offer.