Deep expertise across high-demand therapeutic areas with proven track records
Solid tumors, hematologic malignancies, immuno-oncology, and precision medicine trials.
Alzheimer's, Parkinson's, epilepsy, multiple sclerosis, and psychiatric disorders.
Heart failure, hypertension, arrhythmias, and cardiometabolic disease studies.
Orphan drug development with adaptive trial designs and small patient populations.
Asthma, COPD, pulmonary fibrosis, and respiratory infection trials.
Antiviral, antibacterial, and vaccine clinical trials with rapid enrollment capability.
First-in-human, dose escalation, PK/PD, safety and tolerability studies. 20-100 participants.
Proof-of-concept, dose finding, efficacy and safety evaluation. 100-300 participants.
Pivotal registration trials, multi-regional, large-scale efficacy confirmation. 300-3,000+ participants.
Post-marketing surveillance, real-world evidence, long-term safety monitoring.
Comprehensive clinical research solutions tailored to your needs
Expert medical monitoring, protocol development, and scientific advisory services from experienced physicians and scientists.
Navigating complex regulatory landscapes across multiple jurisdictions with deep local knowledge and global perspective.
End-to-end project oversight ensuring timelines, budgets, and quality standards are consistently met and exceeded.
Robust electronic data capture, database design, and data quality management with validated systems.
Statistical analysis plans, interim analyses, and comprehensive reporting by experienced biostatisticians.
Rigorous quality management systems ensuring compliance with ICH-GCP, FDA, and EMA guidelines.
Outsource specific tasks and processes within the tools, systems and management of the client. Out-tasking helps to augment labor capacity within the current operating model without adding headcount.
We understand your project, define the scope, and create a detailed roadmap.
We prepare submission dossiers and manage communications with regulatory authorities.
We manage clinical studies, collect data, and ensure quality control.
We complete statistical analyses and deliver comprehensive final reports.
What sets us apart in the competitive CRO landscape
Operating worldwide with deep local expertise and established site networks in key therapeutic areas.
Agile and adaptive approach that scales to meet the unique demands of each clinical program.
Unwavering commitment to the highest quality standards with robust QMS and continuous improvement.
Proven track record in managing complex, multi-regional studies with demanding protocols.
We are excited to connect with you, understand your goals, and explore how we can support your needs.
Atatürk mah. Ataşehir Blv.
Gardenya 3 Plaza, No:20/32
Ataşehir, 34758 İstanbul
Partner with Atlant Clinical for reliable, high-quality clinical research services across the globe.
Tell Us About Your Project