About Rho, Inc.
Rho, Inc. is a leading clinical research organization that provides innovative solutions to the pharmaceutical and biotech industries. With over 35 years of experience in the field, Rho has established itself as a trusted partner for companies looking to conduct clinical trials that are efficient, cost-effective, and compliant with regulatory requirements.
At Rho, we understand that conducting clinical trials can be a complex and challenging process. That's why we have assembled an integrated team of experts who work together seamlessly to ensure consistent trials that run smarter and more efficiently from development through submissions and publishing.
Our team includes experienced project managers, data managers, statisticians, medical writers, regulatory affairs specialists, quality assurance professionals, and other experts who bring their unique skills and perspectives to every project. By working collaboratively across disciplines and leveraging the latest technologies and methodologies in clinical research, we are able to deliver high-quality results on time and within budget.
One of our key strengths is our ability to provide customized solutions tailored to each client's specific needs. Whether you are a small startup or a large multinational corporation, we have the expertise and flexibility to design a trial strategy that meets your goals while minimizing risk.
We offer a wide range of services across all phases of drug development including protocol development; site selection; patient recruitment; data management; statistical analysis; medical writing; regulatory submissions; safety monitoring; pharmacovigilance; post-marketing surveillance; health economics outcomes research (HEOR); real-world evidence (RWE); market access consulting (MAC); patient engagement strategies (PES) among others.
Our commitment to quality is reflected in our ISO 9001:2015 certification which ensures that our processes meet international standards for quality management systems. We also adhere strictly to Good Clinical Practice guidelines set forth by regulatory agencies such as FDA/EMA/ICH etc., ensuring compliance with all applicable regulations throughout the trial lifecycle.
In addition to our core services in clinical research,Rho also offers specialized expertise in areas such as rare diseases/orphan drugs , oncology/hematology , vaccines/infectious diseases , neurology/CNS disorders , dermatology/skin disorders among others . Our team has extensive experience working with these therapeutic areas which allows us not only provide expert guidance but also accelerate timelines due their complexity .
At Rho Inc., we pride ourselves on being more than just another vendor – we strive for true partnership with each client by providing exceptional customer service at every step along the way. Our goal is not just meeting expectations but exceeding them by delivering high-quality results on time within budget while maintaining open communication channels throughout entire process .
In conclusion,Rho Inc.'s integrated approach combines scientific rigor with operational excellence resulting in successful outcomes for clients worldwide . If you're looking for an experienced partner who can help you navigate through complex challenges associated with drug development then look no further than Rho Inc.!