About Nuvaclin

A modern SMO built on discipline and care

Nuvaclin Research is a professional Site Management Organization (SMO) dedicated to advancing clinical research with precision, compliance, and compassion.
Established in 2025 at Srikakulam, the company bridges the gap between hospitals, sponsors, and investigators to ensure high-quality clinical trial execution.

At Nuvaclin Research, we offer a structured, quality-driven environment for both fresh graduates and experienced professionals to build meaningful careers in clinical research. Our teams gain hands-on exposure to clinical trial operations, regulatory and ethics processes, and quality management systems in alignment with global CRO standards. We seek motivated individuals who value integrity, collaboration, and continuous learning and who are committed to delivering ethical, compliant, and patient-centric research outcomes.

Join us to grow your expertise and contribute to advancing clinical research excellence.

Our Mission

To conduct ethical clinical research with integrity, delivering accurate, high-quality data that meets global standards.

Our Vision

To build long-term partnerships with sponsors and CROs by delivering consistent, compliant, and scalable site management solutions across the therapeutic areas.

Leadership

Linkedin

Dr. Pentapalli V. N. S. H. Vardhini

Managing Director

Vardhini is the Managing Director of Nuvaclin Research, bringing strong academic expertise and growing professional experience in clinical research. She holds a Doctor of Pharmacy (Pharm.D) degree and has been actively involved in clinical research since 2023, with a focused interest in advancing ethical, high-quality clinical trials. Vardhini has completed specialized training in clinical research, gaining hands-on knowledge in clinical trial conduct, regulatory requirements, documentation, and quality management systems. Her leadership approach emphasizes scientific integrity, regulatory compliance, and patient safety, ensuring that all research activities align with global standards.

Linkedin

Mr. P. Praveen Kumar

Co-Director and Head of Operations

Praveen is the Co-Director and Head of Operations at Nuvaclin Research, bringing strong operational expertise and hands-on experience in clinical research. He holds a Bachelor of Pharmacy (B.Pharmacy) degree and has developed practical experience across multiple aspects of clinical trial operations. With a solid understanding of clinical research workflows, Praveen plays a key role in ensuring the smooth execution of studies, operational efficiency, and adherence to regulatory and quality standards. His experience spans study coordination, site operations, documentation management, and process optimization.

Patient Recruitment and Retention

We deliver ethical, efficient, and participant-focused recruitment strategies that support timely enrollment, strong engagement, and high-quality study outcomes.

Patient Recruitment and Retention

Recruitment Strategies

  • Feasibility-driven patient identification
  • Collaboration with investigators and healthcare providers
  • Community outreach and awareness initiatives
  • Use of ethically approved recruitment materials
  • Pre-screening and eligibility assessment

Retention Approach

  • Regular follow-ups and appointment reminders
  • Flexible scheduling to support participant convenience
  • Continuous communication and study updates
  • Addressing participant concerns promptly and respectfully
Patient Recruitment and Retention

Compliance & Quality

We strictly adhere to national and international regulatory guidelines, ensuring that all studies are conducted ethically and responsibly.

Compliance Framework

  • Adherence to ICH-GCP guidelines
  • Compliance with CDSCO and applicable local regulatory requirements
  • Ethics Committee (EC) submission and approval support
  • Continuous alignment with evolving regulatory expectations

Quality Management System

  • Well-defined Standard Operating Procedures (SOPs)
  • Internal audits and compliance checks
  • Audit readiness for sponsor and regulatory inspections
  • Corrective and Preventive Action (CAPA) implementation
  • Continuous quality improvement initiatives

Our Promise

  • Precision in every trial
  • Passion for every patient.
  • Partnership with every sponsor.