Rho's full range of CRO services

We're proud to provide CRO services with depth, expertise, and quality

Rho has been supporting clinical research at pharmaceutical, biotech, and medical device companies for more than 25 years and is an expert in providing end-to-end product development services. Rho's distinction also lies in the coordination of large, multicenter domestic and international clinical trial networks for the National Institutes of Health and scientific contributions to major public health research initiatives. Rho's depth of knowledge in the private and public sectors, customer service, personalized approach, and attention to detail are unmatched in the industry. From Phase I to post-approval, Rho's capabilities encompass regulatory affairs, clinical operations, clinical data management, biostatistics, regulatory and medical writing, quality assurance, and more.

Our people provide comprehensive services with a personalized customer focus

Rho was founded on the principles of excellence and respect for people. This mind-set attracted some of the most dedicated clinical research professionals in our industry. The passion of our talented people helps provide a distinct advantage in customer service, personalized approach, and attention to detail to each of our clients.

Clinical Operations

Rho Clinical Operations is where medical monitoring, product safety, clinical monitoring, and project management come together to provide clinical trial management with exceptional customer service. Each division under Clinical Operations strives to create highly collaborative relationships with our clients to deliver fast, successful, and scientifically sound project deliverables.

Biostatistics and Statistical Programming

Our world-class biostatisticians and seasoned SAS® programmers are unmatched in the industry. In addition to trial design and data analyses, Rho's deep expertise extends to randomization, integrated summaries of safety and efficacy, data safety monitoring boards (DSMBs), support of new drug application (NDA) submissions, negotiations with the FDA and other regulatory agencies, and the preparation of manuscripts and abstracts. Rho is one of the most experienced CROs in the world in the development of adaptive clinical trial designs.

Clinical Data Management

Our data experts have unrivaled skill at considering all the variables within a protocol and translating that information into a reliable clinical database, a rigorous edit-check plan, and an effective data-cleaning strategy.

Regulatory Affairs

Our regulatory experts help our customers accelerate timelines, navigate the submission process, and maximize the life cycle of their product.

Data Standards

Our experts drive current and proposed industry standards. They understand the preferred formats for regulatory authorities, including FDA and EMA, the published standards, and the science behind the study, and they have created tools to meet these needs.

Regulatory and Medical Writing

Our highly skilled writers consistently produce clear, concise, and accurate submission-ready documents and dossiers.

Quality Assurance

Our experienced quality assurance (QA) professionals ensure that quality services are delivered in compliance with client-specified criteria and all International Conference of Harmonization/good clinical practice (ICH/GCP) guidelines and federal regulations.

Rho can help with your outsourcing needs. Call us and we’ll show you how.

What’s it like to have Rho as your CRO?

Need guidance navigating through the clinical trial process?

We're proud to provide CRO services with depth, expertise, and quality

Rho has been supporting clinical research at pharmaceutical, biotech, and medical device companies for more than 25 years and is an expert in providing end-to-end services. Rho's distinction also lies in the coordination of large, multicenter domestic and international clinical trial networks for the National Institutes of Health and scientific contributions to major public health research initiatives. Rho's depth of knowledge in the private and public sectors, customer service, personalized approach, and attention to detail are unmatched in the industry. From Phase I to post-approval, Rho's capabilities encompass regulatory affairs, clinical operations, clinical data management, biostatistics, medical writing, quality assurance, and more.

Our people provide comprehensive services with a personalized customer focus

Rho was founded on the principles of excellence and respect for people. This mind-set attracted some of the most dedicated clinical research professionals in our industry. The passion of our talented people helps provide a distinct advantage in customer service, personalized approach, and attention to detail to each of our clients.

Clinical Operations

Rho Clinical Operations is where medical monitoring, product safety, clinical monitoring, and project management come together to provide clinical trial management with exceptional customer service. Each division under Clinical Operations strives to create highly collaborative relationships with our clients to deliver fast, successful, and scientifically sound project deliverables.

Biostatistics and Statistical Programming

Our world-class biostatisticians and seasoned SAS® programmers are unmatched in the industry. In addition to trial design and data analyses, Rho's deep expertise extends to randomization, integrated summaries of safety and efficacy, data safety monitoring boards (DSMBs), support of new drug application (NDA) submissions, negotiations with the FDA and other regulatory agencies, and the preparation of manuscripts and abstracts.

Clinical Data Management

Our data experts have unrivaled skill at considering all the variables within a protocol and translating that information into a reliable clinical database, a rigorous edit-check plan, and an effective data-cleaning strategy.

Regulatory Affairs

Our regulatory experts help our customers accelerate timelines, navigate the submission process, and maximize the life cycle of their product.

Data Standards

Our experts drive current and proposed industry standards. They understand the preferred formats for the FDA, the published standards, and the science behind the study, and they have created tools to meet these needs.

Medical Writing

Our highly skilled writers consistently produce clear, concise, and accurate submission-ready documents and dossiers.

Quality Assurance

Our experienced quality assurance (QA) professionals ensure that quality services are delivered in compliance with client-specified criteria and all International Conference of Harmonization/good clinical practice (ICH/GCP) guidelines and federal regulations.

Rho can help with your outsourcing needs. Call us and we’ll show you how.

What’s it like to have Rho as your CRO?

Need guidance navigating through the clinical trial process?