What we do
We work for, and have preferred supplier status with, some of the world’s leading biotechnology and pharmaceutical companies. Trials are conducted in strict accordance with ICH GCP guidelines, all applicable international and local regulations and legislation, and any requirements specific to the project. Our highly qualified team will:
- Rapidly identify sites in specific countries which best meet your needs throughout the region
- Organize the entire study documentation workflow, including preparation, translation, review and submission
- Plan and manage every aspect of the trial, from start-up to completion
- Provide full monitoring, site management, financial control and logistical support services
Speed and value
We arrange contracts with the study sites and investigators, provide legal/regulatory and marketing support, supply payment control services, and arrange insurance cover for patients and investigators.
We provide data management, including eCRF creation and maintenance; biostatistical analysis, quality control and external audits; GCP training for investigators and non-healthcare professionals; and medical writing, including translation, proofreading, and the drafting of everything from academic papers to promotional materials.
In short, CRO Atlant Clinical offer a comprehensive international capability with one object in mind: to assure the fastest possible time to market at the lowest possible cost.
Our specialists have extensive experience in conducting Phases I-IV clinical trials for different groups of patients (adults, children) in various therapeutic areas:
- Rare diseases