Nuvaclin Research
Precision for Trials. Passion for Care.
Site Management Organisation (SMO) • Srikakulam
Services
At Nuvaclin Research, we provide end-to-end clinical research solutions with a strong focus on quality, compliance, and scientific integrity. Our expertise spans across Phase I–IV clinical trials, supporting sponsors, investigators, and healthcare institutions at every stage of the research lifecycle. We ensure full regulatory compliance in line with national and international guidelines.
Our expertise includes:
Patient recruitment and retention strategies
Trial coordination and documentation management
Ethics Committee submissions and approvals
Regulatory documentation and amendments
Compliance with ICH-GCP, CDSCO, and applicable guidelines
Audit preparation and regulatory inspection support
Adverse event (AE) and serious adverse event (SAE) reporting
Why Nuvaclin?
Commitment to Quality and Compliance
We ensure precision in every step of the process, maintaining the highest standards of quality and compliance across all projects.
Experienced Leadership and Collaborative Team
Our trained team works seamlessly with sponsors and investigators to deliver accurate, timely, and efficient results.
Structured, SOP-Driven Processes
With a structured approach guided by Standard Operating Procedures (SOPs), we guarantee consistency and accountability throughout the study.
Patient-Centric and Ethical Approach
We prioritize patient safety and ethical practices in every phase of research, ensuring the highest standards of care.
Tailored Solutions for Every Study
Understanding that every study is unique, we customize our strategies based on your objectives, therapeutic areas, and sponsor expectations.
Infrastructure
We maintain a well-equipped, secure, and technology-enabled environment that ensures seamless execution of research activities while meeting regulatory and ethical standards.
- Dedicated clinical research workspaces
- Well-organized administrative and documentation areas
- Secure storage for essential study documents
- Controlled-access facilities to ensure confidentiality and data protection
- Temperature-controlled storage units (refrigerators/freezers)
- In-house document archival facility.
- Investigational Product (IP) storage units.
Lab Capabilities
Precision-driven laboratory support including sample processing, clinical pathology, biomarker coordination, data integrity, and regulatory-compliant operations—ensuring reliable outcomes for clinical research.