Ardent Clinical Research Services Pvt. Ltd.
Ardent Clinical Research Services Pvt. Ltd. is one of India's premier providers of integrated clinical research solutions, with a state-of-the-art operational facility based in Pune, Maharashtra, Hyderabad, Telangana.We proudly serve a diverse clientele across the biopharmaceutical, herbal, nutraceutical, medical device, and generic pharmaceutical sectors.
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ABOUT US
Ardent Clinical Research Services Pvt Ltd is one of India’s leading providers of integrated clinical research services having operational facilities in Pune, MH, Hyderabad, Telangana, India followed by Operations can be executed in Malaysia, Philippines, Dubai, Vietnam, part of Europe region as well. We have been successfully serving to a wide range of clientele comprising of biopharmaceutical, Herbal, Neutraceutical, Device companies and generic drug industry.
Our broad spectrum of superior quality services are designed to meet our customers’ specific needs. The team of experts at Ardent offers management and leadership solutions to clinical researchers to ensure that their project starts on the right foot. Apart from a timely start, an efficient execution and delivery of clinical trial projects is ascertained.
We’re equipped with ICH GCP, Standard Operating Procedures (SOPs) and all our clinical trial activities strictly comply with the regulatory principles and guidelines. As we conform to the highest standards of ethics, the patients under investigation can rest assured about their safety and confidentiality.
With our exhaustive investigator database and technical expertise in diverse areas of therapeutic research, we enable faster patient recruitment, cost-effective trials and a world-class clinical support. But what really sets us apart from our peers is our quick turnaround times and the personal attention, we pay to our customers.
Our Mission
At Ardent Clinical Research Services, our mission is to provide a reliable and supportive ecosystem for clinical trials, experimental research, and observational studies. We tailor each project to the specific needs of our clients, aiming to address the growing global burden of disease and the escalating demand for innovation in pharmaceuticals and medical devices.
Our Vision
We envision a future where Ardent plays a pivotal role not just in the development of new drugs, diagnostics, and therapeutic approaches, but also in shaping the broader healthcare landscape. Our goal is to contribute meaningfully to healthcare planning, promote the continuous evaluation of medical practices, and enhance the overall quality of care through a deep and data-driven understanding of risk factors and health outcomes.
Our Core Values
What ARDENT Stands For
At Ardent Clinical Research Services, our name embodies the values we live by every day. Each letter of “ARDENT” reflects a foundational principle that drives our commitment to excellence in clinical research.
A – Attention to Detail
We ensure meticulous attention to every detail, carefully reviewing and understanding client requirements to deliver precise and reliable results.
R – Responsibility
We uphold our responsibility to society and the people we serve, believing that ethical conduct and social awareness are marks of a truly good organization.
D – Diversity
Our team is made up of individuals from diverse backgrounds and regions across India, fostering inclusive growth and innovation.
E – Excellence
We strive for excellence not by doing different things, but by doing things differently—with innovation, quality, and integrity at the core.
N – Nobility
We are guided by noble values and strong ethics, which we uphold proudly in every aspect of our organizational culture.
T – Teamwork
We believe in absolute teamwork. Our culture supports and encourages participation and feedback at all levels, ensuring collaboration across all functions.
Mr. Chandu Gangadhar Devanpally
Founder & Managing Director
Ardent Clinical Research Services Pvt. Ltd.
Mr. Chandu Gangadhar Devanpally is the visionary Founder and Managing Director of Ardent Clinical Research Services Pvt. Ltd. He holds a Postgraduate degree in Biochemistry and a Diploma in Clinical Research from Nagpur, Maharashtra.
Mr. Devanpally began his career in 2007 in the Department of Clinical Trials at Sushrut Hospital and Research Center, Nagpur. Since then, he has built a dynamic and diverse career in the clinical research industry, working across multiple roles such as Clinical Research Coordinator (CRC), Clinical Research Associate (CRA), Quality Manager, and Operations Manager for both domestic and global clinical trials.
A meticulous and goal-oriented entrepreneur, he has not only contributed to clinical research but has also successfully launched various ventures across different industries. His hands-on experience spans end-to-end clinical trial project management, data management, monitoring, business development, and sponsor/vendor communications.
Mr. Devanpally is a keen strategist with a deep understanding of the evolving research landscape. He brings strong capabilities in protocol-based trial management, team leadership, and training of subordinates, making him a key driving force behind Ardent's growth and reputation.
With outstanding communication, relationship management, and organizational skills, he continues to lead Ardent Clinical Research Services with a commitment to quality, innovation, and ethical excellence in clinical trials.
format_quoteLeading with integrity, innovation, and impact across the clinical research ecosystem.
Ms. Swati Kurandale
Head Clinical Operations and CDM
Ardent Clinical Research Services Pvt. Ltd.
Ms. Swati Kurandale is the Director of Clinical Operations and Data Management at Ardent Clinical Research Services, bringing over 8.8 years of progressive experience in clinical research and clinical data management. She has played a pivotal role in leading global Phase III studies across therapeutic areas including Cardiology, General Medicine, Nephrology, Diabetology, and Oncology.
With a career spanning multiple roles such as Clinical Research Coordinator, Clinical Research Associate, Clinical Trial Associate, and Data Management Lead, Ms. Kurandale has developed deep expertise in clinical trial execution, data management, regulatory compliance, and quality oversight.
In her leadership role, she is responsible for overseeing data management and clinical operations teams, ensuring adherence to global regulatory standards (ICH-GCP, DCGI, ICMR and 21CFR part 11), and driving operational excellence. She has successfully led multiple database setups, audits, reconciliations, and end-to-end data cleaning activities, while ensuring quality deliverables within timelines.
Ms. Kurandale is known for her strategic vision, team mentorship, and ability to foster client confidence by maintaining transparency, efficiency, and compliance. Her expertise with leading EDC platforms such as Medidata Rave and Veeva EDC, combined with her strong operational acumen, makes her a trusted leader in the clinical research domain.
format_quoteDriving excellence in clinical operations through strategic vision and operational expertise.
Our USPs (What Sets Us Apart)
At Ardent Clinical Research Services, we take pride in offering a unique blend of expertise, efficiency, and excellence that distinguishes us in the clinical research landscape. Our key strengths include:
Highly Skilled Investigators
Our team includes experienced investigators with a strong clinical and scientific foundation.
Deep Technical Expertise
We bring in-depth knowledge across a wide range of therapeutic research areas, ensuring scientifically robust study execution.
Advanced IT & Data Management Systems
Our cutting-edge IT infrastructure supports efficient, accurate, and secure clinical data handling.
Access to Ethnically Diverse Patient Populations
Our wide-reaching network allows recruitment from varied demographics, enhancing the relevance and generalizability of study results.
Faster Patient Recruitment
With our established site relationships and vast volunteer database, we ensure swift and efficient patient enrolment.
Cost-Efficient Clinical Trials
We deliver high-quality services while maintaining budget-friendly solutions for our sponsors.
High-Quality Output
Quality is at the core of everything we do—from protocol design to final study reports.
World-Class Clinical Support
Our dedicated teams offer continuous support across all phases of the trial lifecycle.
Conducive Environment for Clinical Trials
We provide a well-regulated, ethically sound, and operationally efficient setting for clinical research.
Quick Turnaround Time
We value time and are committed to delivering results within aggressive timelines.
Customer-Centric Approach
Every project is handled with minute attention to detail and a deep understanding of client-specific requirements.
International Collaborations
Expanding clinical research capabilities through strategic partnerships across four continents
Hungary
Europe Region
Collaborated with a reputed European CRO to support clinical research activities across the European market, with Hungary as a regional hub.
Malaysia
Southeast Asia
Partnered with CRM Malaysia to enhance capabilities in clinical trial operations and regulatory alignment within Southeast Asia.
Vietnam
Southeast Asia
Established a collaboration with a leading Vietnam-based CRO to support therapeutic research and patient recruitment across the Vietnam region.
Sri Lanka
South Asia
Teamed up with Sri Lankan Site Management organizations to support study sites, investigator engagement, and local trial oversight in Sri Lanka.
Philippines
Southeast Asia
Teamed up with reputed Philippines CRO to support clinical research activities across the Philippines region.
Dubai
Middle East
Ardent and Sourcretranscript together registered a company as a CRO in Dubai for the Middle east region clinical operations.
Our Reach, Strength & Recognition
At Ardent Clinical Research Services, our numbers speak for our capabilities and commitment to excellence in the clinical research domain.
Excellence Across India
Nationwide clinical research network
Our extensive network and proven track record demonstrate our commitment to delivering exceptional clinical research services across India, backed by world-class infrastructure and expertise.
100+ Clinical Trial Sites Nationwide
We have established a strong presence across India with over 100 clinical trial sites, enabling broad access to diverse patient populations and ensuring effective multi-center study execution.
500+ Experienced Investigators
Backed by a network of more than 500 doctors across various therapeutic areas, we bring unmatched medical expertise and clinical depth to every study we undertake.
10 Specialized Departments
Our organization is structured into 10 distinct departments, each led by experienced professionals, covering every aspect of clinical research — from project management to pharmacovigilance and regulatory affairs.
12+ Prestigious Awards
We are proud to have been recognized and awarded 9 times for our excellence, innovation, and contribution to the field of clinical research. These accolades reflect our dedication to quality and ethical conduct.
Quality in Services Is Paramount for Us
At Ardent Clinical Research Services, quality is the cornerstone of our operations. We are committed to delivering excellence by strictly adhering to international regulatory standards, including:
- fiber_manual_recordICH-GCP, US FDA, EMEA guidelines, and India's New Clinical Trial Rules, 2019
- fiber_manual_recordEthical and scientifically sound investigations across all phases of clinical research
- fiber_manual_recordA robust Quality Assurance System that actively monitors and ensures compliance with our Standard Operating Procedures (SOPs)
- fiber_manual_recordWell-defined Quality Manuals, regular Quality Audits, and Continuous Staff Training to maintain high performance and consistency
- fiber_manual_recordExtensive global regulatory expertise in medicinal product testing, manufacturing, and regulatory submissions
Our uncompromising focus on quality ensures reliability, compliance, and trust in every project we undertake.