Full-Service CRO's
Clinical Trial Management from Start to Finish
At Sanos, we offer full-service CRO solutions, managing every aspect of clinical trials from study feasibility and protocol design to regulatory affairs, risk-based monitoring, and statistical analysis. Our expertise spans early-phase development through large-scale, late-phase trials, ensuring seamless execution at every stage.
With a focus on data integrity, operational efficiency, and regulatory compliance, we optimize study outcomes while mitigating risks. Whether managing pharmacovigilance, IMP logistics, or patient recruitment, we ensure trials are conducted with precision, transparency, and a commitment to scientific excellence.
Musculoskeletal and Related Disorders
NBCD
With 20+ years of experience, NBCD is a trusted partner in musculoskeletal clinical trials. Highly specialized in musculoskeletal and related disorders, they lead innovation through precise trial execution.
Neurological Disorders
Neuroscios
Neuroscios is experts in neurological clinical research, with more than 30 years’ experience – pioneering advancements in Alzheimer’s and CNS disorders with deep scientific insight.
Dermatological Conditions
Blueskin
Deeply focused on dermatological clinical research, Blueskin delivers high-quality, patient-centered trials in skin disease research.
The People Running Your Study
Clinical Trial Managers
Our CTMs bring strong operational expertise and lead all trial activities with precision and ownership. With experience in risk-based monitoring and site management, they combine scientific insight with hands-on coordination to ensure efficient and compliant study delivery.
Clinical Research Associates
Our CRAs are more than monitors – they’re trusted site partners and valued members of our operational teams. In addition to feasibility and monitoring, they support site payments, centralized oversight, and sponsor collaboration, always ensuring data integrity and patient safety.
Clinical Data Managers
Our data managers deliver tailored, high-quality solutions that support clinical research from database build to submission. With in-house programming, biostatistics, and ePRO/eCOA expertise they help sponsors capture clean, meaningful data across every phase.
Regulatory Affairs & Pharmacovigilance
Our Regulatory team manages global submissions with accuracy and speed, working across EMA, FDA, MHRA, SFDA, and more. On the safety side, our PV experts handle all clinical trial safety tasks, either independently or in collaboration with sponsor teams.
Quality Management Team
Our QMS is based on ISO 9001 and built for risk-based oversight, subject safety, and regulatory readiness. The team works closely with operations to uphold data quality and compliance, drawing on experience from audits, inspections, and system design.
Science & Medical Team
Our science team drives the design of high-quality, scientifically sound trials across our therapeutic focus areas. With deep scientific knowledge and experience mitigating placebo response, they work closely with sponsors to design trials that are both rigorous and relevant.