About Us
Who We Are
About CliniGlia
At CliniGlia Research Solutions Private Limited, we believe that every site tells a story — and we’re here to make sure yours is managed with precision, care, and vision.
Founded with a passion for streamlined operations and sustainable growth, we specialize in end-to-end site management solutions that keep your projects running smoothly, on time, and within budget. From planning and compliance to maintenance and optimization, our team ensures every detail is handled with expertise.
At CliniGlia Research Solutions Private Limited we don’t just manage sites — we build trust, ensure efficiency, and create lasting value.
- Pharmaceutical Companies
- Allied Medicine Companies
- Biotechnology Companies​
- Medical Device Companies
- Phytopharmaceutical Companies
Who We Are
About CliniGlia
At CliniGlia Research Solutions Private Limited, we believe that every site tells a story — and we’re here to make sure yours is managed with precision, care, and vision.
Founded with a passion for streamlined operations and sustainable growth, we specialize in end-to-end site management solutions that keep your projects running smoothly, on time, and within budget. From planning and compliance to maintenance and optimization, our team ensures every detail is handled with expertise.
At CliniGlia Research Solutions Private Limited we don’t just manage sites — we build trust, ensure efficiency, and create lasting value.
- Pharmaceutical Companies
- Allied Medicine Companies
- Biotechnology Companies
- Medical Device Companies
- Phytopharmaceutical Companies
Mr. Chandrakant Vikram Wagh
Dr. Sapna Chandrakant Wagh
Director Profile
Hands-On Clinical Research Experience Since 2007
Our founder-director brings direct experience of running clinical studies at site level, registration and administration of ethics committees, facing regulatory audits, and training research teams. That experience shapes how CliniGlia plans and supports every trial.
With a strong understanding of clinical research operations and Indian & Global regulatory requirements, our leadership focuses on practical, quality-driven trial execution. This hands-on experience helps CliniGlia anticipate challenges, strengthen site readiness, and maintain compliance throughout the study.
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National and Multinational Phase II to IV studies, pilots and registries across various indications
Ethics committee registration and administration since 2013
Faced Sponsor, DCGI and NABH audits
Faculty for GCP, ICH-GCP, ICMR, Regulatory Changes and updates, NDCT Rules 2019 and NABH accreditation training
Our Vision & Mission
What we work towards, and how we hold ourselves to it.
Our Vision
Treatments Reaching Patients Sooner
To make new treatments available to patients earlier than is the case today, without administrative or cultural barriers slowing the way.
Matching clinical trial sites to the needs of each study protocol is at the heart of our efforts. It benefits patients, and it gives Sponsors and CROs projects they can rely on to run on time and on budget.
Our Mission
Our Commitments
To build a strategic partnership with selected Sponsors and CROs.
To provide quality services to the healthcare industry in the field of clinical research.
To provide quality therapeutics to improve human lives.
Our Strengths
Excellence in Clinical Research
A full range of SMO services, delivered by a dedicated team that works alongside Sponsors and CROs from feasibility to site close-out.
Faster Patient Recruitment
Networks of qualified patient pools and quick follow-up help us attract and retain patients more effectively than internal teams.
Improved Data Management
Technology and data-handling processes for clinical and regulatory data reduce study delays.
Focused Research
We take on the routine site work so research teams can spend their time on the data that matters.
Shorter Timelines, Lower Cost
End-to-end support from setup to close-out, in line with GCP, Indian and Global regulatory standards, keeps studies on schedule and on budget.
Our Strengths
Why CliniGlia
A full range of SMO services, delivered by a dedicated team that works alongside Sponsors and CROs from feasibility to site close-out.
Faster Patient Recruitment
Networks of qualified patient pools and quick follow-up help us attract and retain patients more effectively than internal teams.
Improved Data Management
Technology and data-handling processes for clinical and regulatory data reduce study delays.
Focused Research
We take on the routine site work so research teams can spend their time on the data that matters.
Shorter Timelines, Lower Cost
End-to-end support from setup to close-out, in line with GCP, Indian and Global regulatory standards, keeps studies on schedule and on budget.
20+
EC Registrations
300+
Subjects Recruited
11+
Regulatory, Sponsor & NABH Audits
30+
Trainings & Indian / International Conferences