Geographic Reach

In the ever-evolving landscape of clinical research, geographic reach plays a pivotal role in the success and efficiency of clinical trials. A broad geographic footprint ensures diverse participant recruitment, robust data collection, and comprehensive market representation. At Catawba Research, we understand the critical importance of this aspect, leveraging our expansive presence to deliver unparalleled clinical trial services.

Global Headquarters and Operations

Catawba Research is strategically headquartered in Charlotte, North Carolina, and Mumbai, India. This dual-headquarter model allows us to bridge the gap between Western and Eastern markets, facilitating seamless collaboration and access to diverse patient populations.

Comprehensive Service Offering

We pride ourselves on offering both full-service and functional-service outsourcing. Our internal capabilities extend across the United States, Canada, Central America / Caribbean, and India. Outside of these regions we work with qualified and approved partners in Europe, Asia, and Australia to enable our comprehensive geographic coverage. This extensive geographic reach enables us to provide tailored solutions that meet the unique needs of each trial, ensuring sponsors receive the highest quality data and regulatory compliance.

Diverse and Expert Team

Our team comprises industry Subject Matter Experts (SMEs) with global regulatory and operational expertise. This diversity in expertise ensures that we can address the complexities of clinical trials across therapeutic areas and regulatory environments. Our SMEs bring local knowledge and global insights, facilitating the successful execution of trials in any region.

Benefits of Geographic Reach

1. Global Patient Access

Our global capabilities enables us to recruit subjects successfully by accessing countries where disease prevalence and incidence are higher, patient access to approved therapies is lower, and access to healthcare services is lower. In these areas patients are often more willing to participate in clinical trials to receive cutting-edge treatments. This dynamic accelerates recruitment by tapping into populations with a greater need for new therapies and to use research to help address unmet medical needs in underserved areas.

2. Diverse Participant Recruitment

A broad geographic reach allows for the inclusion of diverse participant populations, leading to more generalizable and robust study outcomes. This diversity is crucial for understanding how treatments perform across different demographics and geographies.

3. Efficient Data Collection

With operations spanning multiple regions, we can collect data more efficiently and from a wider array of sources. This enhances the reliability and validity of study results, providing a more comprehensive understanding of treatment effects.

4. Regulatory Compliance

Navigating the complex regulatory landscapes of different countries requires local expertise. Our global presence ensures that we can efficiently manage regulatory submissions and compliance, reducing delays and enhancing the speed of trial completion.

5. Market Representation

Conducting trials in various regions ensures that the study results are representative of the global market. This is particularly important for sponsors looking to launch products internationally, as it provides valuable insights into how treatments will perform in different markets.

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