What we do
At Atlant Clinical, we work hand-in-hand with the world’s leading biotech and pharmaceutical companies. Our preferred supplier status with some of the biggest names in the industry confirms we have the insight and daily experience to manage your project with utmost efficiency.
Trials are conducted in strict accordance with ICH GCP guidelines, all applicable international and local regulations, and any project-specific requirements. Our extremely qualified and knowledgeable team will:
- Quickly identify a variety of sites in individual countries which best meet your needs
- Organize the entire study documentation and workflow – including preparation, translation, review, and submission
- Plan and manage all aspects of the trial, from beginning to completion
- Provide full monitoring, site management, financial control, and logistical support services
Speed, Value, and Diligence
Atlant Clinical arranges all contracts with study sites and investigators and provides legal and regulatory support. We organize marketing, supply payment control services, and set up insurance for patients and investigators.
We offer a multitude of data management tools, including eCRF creation and maintenance. We coordinate external biostatistical and quality control analysis, as well as GCP training for investigators and non-healthcare professionals. We also provide medical writing services – from simple translation and proofreading, to the creation of academic papers and promotional materials.
CRO Atlant Clinical is the single choice for comprehensive, international clinical trials. And we always keep our eye on the end goal: assuring our clients’ products get to market in the shortest possible time, at the lowest possible cost.
Our specialists have extensive experience conducting Phases I-IV clinical trials for all types of patient groups and a vast range of therapeutic areas. Our specific fields of expertise are (though not limited to):
- Rare diseases