Clinical Trial SMO Services
Comprehensive Site Management Solutions for Clinical Trials
Discover the Power of Clinical Excellence
At Vivoclin Research SMO Division, we provide end-to-end Site Management Organization (SMO) services to streamline your clinical trials. From site selection and patient recruitment to regulatory compliance and quality assurance, our services are designed to ensure the success of your studies while reducing operational burdens for sponsors and CROs.
Let's ConnectRedefining Clinical Research Excellence
We specialize in optimizing clinical trial operations through expert site management, quality compliance, and efficient processes. Our experienced teams work collaboratively to ensure successful trial outcomes while maintaining the highest industry standards.
Pioneering Clinical Excellence
We are a trusted leader in clinical research across India, working with dedication and precision to advance healthcare
Expertise Across Core Units
Our experienced teams provide complete research solutions through strong partnerships, ensuring high quality and reliable results
Comprehensive Service Portfolio
We offer complete support from start to finish, helping manage participants, schedules, and providing round-the-clock assistance to ensure smooth operations
Global and Local Reach
We work with clients worldwide while maintaining strong local connections, helping advance medical research at all stages
Therapeutic Specialization
Our research covers many medical areas including cancer, lung health, heart conditions, and brain disorders, with a personalized approach for each study
Collaborative Partnerships for Success
We work closely with many healthcare partners to improve research quality and achieve better results for patients
Our Core Expertise
Site Identification & Feasibility
Selecting optimal sites based on protocol needs, infrastructure, and investigator expertise.
Site Setup & Initiation
Managing regulatory approvals, site activation, and investigator training for compliance.
Patient Recruitment & Retention
Implementing digital strategies and outreach programs to enhance enrollment and retention.
Regulatory Compliance & Ethics
Ensuring adherence to ICH-GCP, FDA, and local guidelines with complete documentation.
Our Services
We offer a comprehensive portfolio designed to optimize your clinical research journey
Site Coordination
Schedule management, subject recruitment, AE/SAE reporting, and more.
Site Management
Ensuring operational efficiency with services such as data entry and equipment management.
Reporting
IRB submissions, protocol deviation reporting, and full regulatory compliance.
Contact Center
A 24-hour call center (coming soon) for real-time responses, privacy consultations, and query handling.