Contacts
Unit 863, Cospacio: Premium Coworking,
8th Floor, Celica Park, 24, Park Street Park
Center, Kolkata, West Bengal 700016
OrciVita Sciences & Research Pvt. Ltd. is a leading Site Management Organization (SMO) established in 2019, committed to delivering high-quality, ethical, and patient-centric clinical research services across India. We partner with Global and Indian Sponsors, CROs, and investigators to ensure seamless execution of clinical trials in compliance with ICH-GCP, NDCT Rules 2019, and other local regulatory requirements.
With a strong operational foundation and a growing site network, OrciVita plays a critical role in bridging the gap between bench to bedside.
Currently operational at multiple sites at Kolkata and Bhubaneswar, advancing our footprints to other states in the near future. Worked on more than 60 studies of which 35 are already archived.
To be a trusted and preferred clinical research SMO partner in India by enabling efficient, compliant, and high-quality clinical trials that contribute to scientific advancement and improved patient outcomes.
- To support sponsors and CROs with reliable site-level execution
- To ensure patient safety, data integrity, and regulatory compliance
- To empower investigators and site teams through training, systems, and operational excellence
- To strengthen India’s clinical research ecosystem with ethical and transparent practices
Tirna Halder founded OrciVita Sciences & Research Pvt. Ltd. in 2019, bringing with her over 7 years of hands-on field experience across multiple therapeutic indications. The vision behind building the OrciVita brand was to deliver high-quality, ethical, and compliant clinical research in India while strengthening site-level execution.
With extensive experience in clinical trial operations and site management, Tirna has been instrumental in establishing OrciVita as a trusted partner for sponsors, CROs, and investigators. Her expertise includes study startup activities, site activation, patient recruitment and retention, documentation excellence, along with regulatory and ethics coordination, ensuring smooth, efficient, and audit-ready trial execution. She is widely recognized for her strong attention to detail and her ability to translate complex clinical protocols into practical, site-friendly processes that support investigators, study team, and patients.
As a leader, Tirna firmly believes that quality clinical research begins at the site level. She prioritizes ethical conduct, patient safety, data integrity, and continuous training of site teams. Under her leadership, OrciVita has developed a culture rooted in compliance, accountability, and operational excellence.
In addition to her leadership role, Tirna is highly academically oriented. She is currently pursuing a PhD in Biotechnology and holds one patent, along with 17 national and international scientific publications. With a professional career spanning 13 years, she has also served as a presenter and speaker at several national and international conferences, contributing actively to the scientific and clinical research community.
OrciVita has developed deep expertise in end-to-end site management, with a focus on operational excellence and quality
Our team has experience supporting studies across multiple
therapeutic areas, including but not limited to:delivery.
Separate Operations Quality, Feasibility and study start up departments to ensure data integrity, quality and smooth feasibility to site initiation experience for both Sponsor CRO and site.
Pan India Tie up with Oncquest Laboratories Pvt. Ltd. for laboratory services and Crown Worldwide Pvt. Ltd. for archival services.
Proven operational capability since 2019
Reliable execution at the site level
Strong focus on quality, timeliness, and compliance
Transparent communication with sponsors and CROs
Commitment to long-term partnerships rather than transactional engagement
At OrciVita, patient safety and data integrity are non-negotiable. Every study is executed with strict adherence to ethical standards, regulatory guidelines, and sponsor expectations. Our SOP-driven framework ensures consistency, audit readiness, and continuous improvement across all projects.
As clinical research evolves, OrciVita continues to strengthen its site network footprint, adopt technology-enabled processes, and invest in training and leadership development to support increasingly complex trials in India.
Supporting clinical trials for sponsors and CROs worldwide.
