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Full-Service Global CRO

Catawba Research, LLC (CR) is a full-service contract research organization (CRO) providing clinical management services to pharmaceutical, device, formulation development and biotechnology companies. We focus on what we know best: dermatology, women’s health, ophthalmology, gastroenterology and respiratory.
Introducing Catawba Research India

Catawba Research India Opens Doors
For Clinical Trial Data Management

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Cruising Through the World of 505(b)(2)s

In this episode of Catawba In Focus, we head over to visit Tom Filipczak – managing director and partner at Destum Partners. Tom chats with Zaidoon about industry deals during a global pandemic and what that looks like on the 505(b)(2) side of things. We also swing by "the shop" to talk with Billy the mechanic about overhauling Catawba Research's famous red truck – Uma. While the classic Chevrolet Apache is getting some improvements and upgrades, it's still the same vehicle...much like that of a 505(b)(2)! Hop in and join us.

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Behind The Scenes Of Study Start-Ups

On this episode of Catawba Talks, we sit down to discuss the intricacies of study start-ups with Catawba Research's Clinical Project Manager, Chris Driskill, and Director of Clinical Operations, Caryn Thompson. Listen as we dig into the challenges and wins of launching a new trial. Trust us, this episode is packed with inside info on the entire process! We'll cover some of the key differences between Phase 2 and Phase 3 study start-ups and the stress-inducing world of EDC (Electronic Data Capture) logistics! From vendor setup to site contracting and more, we've got you covered. Join us. PS. Chris is feeling MUCH BETTER (listen to the episode, and you'll know what we're talking about!)

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Catawba Confidence

A global contract research organization
taking on today's clinical trials in a new way.

Catawba Research is a contract research organization providing clinical trial management services to pharmaceutical, device, formulation development and biotechnology companies. We conduct and manage clinical trials in accordance with the International Conference on Harmonization-Good Clinical Practices (ICH-GCP) and all other applicable regulatory requirements.

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