Clinical Research Services
Delivering excellence across all spheres of clinical trial processes with customized solutions for our clients
Our Core Services
SMO-India offers the below mentioned services to cater our client's clinical trial requirements
Feasibility Studies
Site Selection & Onsite Trial Management
Project Management and Monitoring for Phase Clinical Trials
Patient Recruitment & Retention Strategies
Clinical Quality Assurance
Regulatory Support
Ethics Committee Services
Clinical Trial Staff Support
Data Management at Site
Training & Education
Our Key Strengths
What sets us apart in clinical research excellence
Network of experienced physicians and coordinators across India, which is continuously expanding
Excellence in Onsite Coordination and Monitoring of Phase I, II, III, and IV clinical trials
Leadership and management expertise necessary to produce consistent and statistically sound data for every study conducted
Multiple Therapeutic Segments coverage
Streamlined and expeditious start-up and completion of studies on schedule
Large and diverse patient population with a positive attitude towards clinical research
Dedicated full time certified Clinical Research Coordinators experienced in working with Pharmaceutical companies and Contract Research Organizations
Quality source documentation, case report forms and other paperwork
Sites that are top enrollers nationwide on multiple studies by virtue of their inherent merits
Centralized organizational Structure offers Sponsor and CRO clients immediate access to several pre-qualified investigators in all therapeutic segments
Advanced Clinical Trial Database
To improve current standards as well as the overall standards of Clinical Research, we are constantly developing a clinical trial database at the site level as well as central level at headquarters. This serves as a quick, efficient and effective tool to deliver accurate, precise feasibility analysis.
Thus SMO-India is becoming reliable partner for Sponsor/CRO in conducting multicentric clinical trials. This also helps to efficiently organize the total clinical trial process, both centrally (HQ) and locally (Site). Our organizational structure offers Sponsor and other clients immediate access to several pre-qualified investigators in all therapeutic segments.
Proven Track Record
Our achievements in clinical research excellence
- Clinical Trials as SMO
- 115+
- Years Experience
- 25+
- Full-service CRO Trials
- 14+