(Site Management & Development Organization) by a group of experienced Clinical and Healthcare professionals.
Why SMO... What We Do
-Ultimately, reducing overall costs per valid data set
-Shortening time to reach given milestones
-Improving data quality
-Increasing resource-utilization
-Efficiency
-Improving communication
Clials Advantage
-Record of Quality
-Flexible Approach
-Dedicated People
-Fast Timelines
-Broad TA Expertise
providing workforce for repetitive and administrative tasks
taking particular care of defined timelines and all required changes
and updates; coordinating multi-party communication between the center, the CRO and the sponsor;
Healthcare field attracts to save lives & helping people, being a doctor is not your only choice. We how else you can help patients without being a doctor, here we serving awesome opportunity.
Neurology
Dentistry
Dermatology
Endocrinology
Gastroenterology
OB & Gynecology
Opthalmology
Orthopedics
Oncology
Otolaryngology
Cardiovascular Diseases
Neurological Surgery
Hematology
Internal Medicine
Nephrology
Pediatrics
Psychiatry
Pulmonary Disease
Rheumatology
Urology & General Surgery
Don't hesitate, contact us for better help and services. Explore Us.
SMO Solutions
CLIALS supports clinical trials by placing highly trained Clinical Research Coordinators (CRCs) at each research site dedicated to a specific protocol. CRCs are delegated by PI and mainly support investigators on non-medical-evaluating related study activities during the conduct of a clinical trial.
Interested in CLIALS
CLIALS is a leading SMO that accelerates to contribute to a safer and better world. We do this by combining our 25 years of proven quality and results with expertise in 30+ therapeutic areas, a flexible approach, and dedicated team who enable rapid startups and fast timelines.
Best Services
We are service providers for contract research organizations, pharmaceutical, biotech and medical device companies and even for clinical research sites.Our Study Coordinators will take care of non-medical trial specific processes and tasks to improve the outcome for sponsors and reduce the burden for research teams.
Clinical trials require strict adherence to protocol, extensive documentation, complete accuracy, compliance to ICH-GCP and other regulatory norms, an ethically sound patient recruitment strategy, and efficient site management.