About Us
At Advanced Research, we are committed to advancing medical science by conducting high-quality, compliant, and efficient clinical trials that bridge the gap between scientific discovery and real-world treatment solutions. Our expertise ensures that pharmaceutical sponsors and biotech firms have a reliable research partner capable of delivering timely execution, robust patient enrollment, and regulatory excellence.
We take pride in our ability to streamline drug development by combining cutting-edge research methodologies with a patient-centric approach. We ensure that every clinical trial is conducted with precision, efficiency, and adherence to the highest ethical and regulatory standards.
Our Process
At Advanced Research, our Standard Operating Procedures (SOPs) and clinical execution processes are meticulously designed to uphold the highest standards of data integrity, regulatory compliance, and patient safety throughout every phase of research.
We implement rigorous quality control measures to ensure that our clinical site operates in strict adherence to Good Clinical Practice (GCP) guidelines and all regulatory requirements. Our structured approach guarantees that every trial meets or exceeds industry standards, fostering reliable, high-quality outcomes that drive medical advancements.
Each member of the Advanced Research team undergoes comprehensive training to execute clinical trials with precision, efficiency, and ethical integrity. By maintaining a steadfast commitment to patient safety and data accuracy, we continuously enhance the credibility and impact of our research operations.
Why Sponsors Choose Us
🔬 Extensive Expertise in Clinical Trials
With years of experience conducting Phase I-IV clinical trials across diverse therapeutic areas, our team of board-certified investigators, research scientists, and clinical professionals brings unmatched expertise to every study. We specialize in protocol adherence, precise data collection, and regulatory compliance, ensuring high-quality outcomes that advance the field of medicine.
📊 Regulatory Excellence & Data Integrity
Our trials strictly follow ICH-GCP, FDA, and IRB regulations, ensuring that every study meets the highest scientific and ethical standards. We prioritize data accuracy, integrity, and compliance, working diligently to eliminate inefficiencies, minimize delays, and optimize approval timelines for novel treatments.
👥 Strategic Patient Recruitment & Retention
We employ innovative, data-driven recruitment strategies, utilizing electronic medical record (EMR) databases, digital outreach, and community-based partnerships to ensure fast and effective patient enrollment. Our strong patient engagement framework fosters high retention rates, significantly reducing dropout risks and enhancing trial success.
🏥 State-of-the-Art Research Facilities
Our advanced clinical research centers are fully equipped with cutting-edge diagnostic tools, on-site laboratories, and dedicated monitoring areas, allowing us to execute trials with seamless precision. Our facilities support a wide range of therapeutic studies, ensuring that sponsors benefit from a highly controlled and resource-rich environment.
🤝 Comprehensive End-to-End Support
From site selection to study closeout, we provide a full spectrum of clinical trial management services, including:
✔ Regulatory submissions and compliance oversight
✔ Site operations and study coordination
✔ Patient monitoring and safety assessments
✔ Real-time data analysis and reporting
At Advanced Research, we are more than just a clinical trial site—we are a strategic partner committed to driving medical innovation and delivering transformative healthcare solutions.
📢 Partner with us to accelerate your drug development pipeline and shape the future of medicine.
Our Team
Dr. Shailesh Gupta
M.D., M.B.A
Dr. Manish Gupta
M.D., FAAOS
Dr. Vivek Sawhney
Vice President
Danahe Navarrete
Chief Operating Officer
Dr. Harshal Sanghvi
Senior R&D, Chair, Dept. of Tech and Clinical Trials