Services
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FSP for Biotech
An FSP model designed for biotech
Functional Service Provider models have long been associated with large pharma companies, outsourcing departments, and off-shoring practices that emphasize low cost over quality and scale over thoughtful program management. -
Marketing Applications
Setting the highest standards for marketing applications
A marketing application is the most critical milestone in your clinical research program. Quality applications can accelerate time to market, bring the benefit of new treatments to patients sooner, maximize research investments, and conserve patent life – demanding a partner with an insider’s understanding of the regulatory landscape and a proven track record for success. -
Program Strategy
Intelligent guidance to catalyze development and chart a strategic path to approval
From preclinical proof-of-concept candidates to approved products primed for post-marketing label extension, our Product Development experts will plan and coordinate each clinical, non-clinical, CMC/Quality, and regulatory activity for your product. We balance risk against accelerated timelines by optimizing regulatory interactions and strategically running the right studies at the right time. Our goal is to create a program strategy that will get your products to patients faster while preventing costly development missteps. -
Biostatistics Services: All Phases of Drug Development
We have proudly delivered expert statistical analyses and programming to all phases of drug development in a wide range of therapeutic areas for over 25 years.
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Clinical Data Management
Fast, flexible, and quality clinical data management
Clinical Data Management has undergone a rapid evolution, and the tools and processes of the last decade are not enough to ensure high-quality clinical data anymore. Grounded in a foundational knowledge of clinical data management best practices, our experts have developed system-agnostic, in-house data visualization and statistically-based anomaly detection and trend identification tools to provide actionable, risk-based insights and ensure the timely and accurate review of clinical trial data. -
Clinical Monitoring and Operations
Strong site relationships and efficient study start-up
Successful study execution requires more than just source data verification (SDV) and on-site clinical monitoring. Our clinical operations team ensures efficient study start-up, quick enrollment, and high quality execution at the site-level through extensive therapeutic and regulatory knowledge, solid training programs, and development of strong site relationships. Our clinical operations experts also have extensive experience designing and executing decentralized and virtual clinical trials. -
Clinical Project Management
Setting high expectations and exceeding them
For more than 30 years, Rho has helped pharmaceutical and biotechnology companies successfully lead their clinical research projects from initiation to closure. Our Project Managers have years of experience managing clinical trials and programs, including decentralized and virtual trials, in our therapeutic areas of expertise, including Neurology, Psychiatry, Analgesia, Rare Disease, and Infectious Disease and Vaccines. This experience has also given them broad knowledge of clinical research which helps to unify their trial teams and deliver results that are within the desired scope, timeline, and budget. -
Consulting
Clinical trials involve a myriad of complicated processes and variables. Rho can help you navigate the clinical trial process to save you time and minimize costs.
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Data Standards
Decades of experience in CDISC standards implementation
We combine our decades of CDISC standards implementation expertise and regulatory experience to produce the highest quality clinical databases that allow regulatory reviewers to focus on your clinical results. -
Global Reach
Clinical trial solutions for your global programs
Our global solutions will ensure you reach your patients, wherever they are. With global capabilities that span 5 continents (North and South America, Europe, Asia, and Australia), we provide full service capabilities to execute your clinical development programs and trials across the globe.