Your Project Partner for Success and Beyond.
Sapientia Medicus Research was founded to address the needs of the pharma and medical devices industry by providing a flexible Site Management Organization (SMO) with therapeutic excellence in Gastroenterology, Ophthalmology Anaesthesiology, Critical Care, Pain, and Preoperative Medicine. Headquartered in Ahmedabad, the Clinical Research Hub of India, Sapientia Medicus Research capitalizes on India’s streamlined regulatory environment, trained professionals, compliant patients, and motivated clinical sites.
As an SMO, we ensure the fastest possible start-up of research sites within our network. Studies cover Phase I - IV and 70% of which are sponsored by global pharma companies.
SMO
Sapientia Medicus Research
Legacy
Pioneering advancements in clinical research, we’ve built a legacy of delivering successful trials with precision and integrity. Our focus on quality continues to shape the future of healthcare.
Journey
Our journey spans years of expertise in managing clinical trial sites across diverse therapeutic areas. With a focus on efficiency and accuracy, we continue to drive innovation and success in every trial.
Code
Integrity, transparency, and patient safety are at the core of our operations. We are committed to ethical research and delivering the highest standards of quality in every project.
Fastest patient enrolment without affecting data quality
Sapientia Medicus Research, as an SMO, plays a crucial role in rescue studies by stepping in to manage and revitalize clinical trials that are at risk of failing. Sapientia Medicus Research provides expert oversight, enhances patient recruitment, ensures regulatory compliance, and improves data quality. By addressing key challenges and optimizing site operations, we ensure that these studies can meet their objectives and be successfully completed within timeline.
We offer invaluable support by easing burdens and ensuring accuracy. Our expertise makes us trusted partners, helping deliver superior trials and ultimately, contributing to medical breakthroughs that improves lives.
Operational Oversight
Ensuring that all activities at the site are conducted smoothly and efficiently, adhering to regulatory requirements and organizational standards.
Resource Management
Coordinating the use of resources such as personnel, equipment, and materials to ensure that the site operates effectively.
Compliance
Making sure that the site complies with relevant laws, regulations, and industry standards. This can include health and safety regulations, environmental regulations, and other legal requirements.
Excellence Assurance
Implementing and monitoring quality control measures to ensure that the work or research being conducted meets the necessary standards and specifications.
Communication
Acting as a liaison between different stakeholders, including sponsor/CRO, EC members, principal investigator, and team members, to ensure clear and effective communication.
Problem-Solving
Addressing any issues or challenges that arise on-site and implementing solutions to keep operations on track.
Documentation
Keeping detailed records of site activities, incidents, and compliance checks to ensure accountability and facilitate reporting.
Our numbers speak for
themselves
10
Therapeutic Areas
50
Studies
100
Clients
2000
Patients
Some of our clients
reviews
I had the opportunity to collaborate with Sapientia Medicus Research on a wet AMD clinical trial involving aflibercept. Their performance was nothing short of outstanding. The trial was completed ahead of schedule, and the quality of the data they provided was impeccable. Moreover, they achieved the highest patient recruitment among all the participating sites, showcasing their extensive network and excellent patient engagement strategies. I would highly recommend Sapientia Medicus Research to anyone looking for a reliable and efficient SMO partner.
I have had the pleasure of collaborating with Sapientia Medicus Research on multiple clinical trials, and I am always impressed by their efficiency and dedication. Their attention to detail and clear communication ensures that each phase of the trial runs smoothly. The team's ability to maintain high recruitment numbers while delivering quality data is impressive. I always trust them to meet deadlines and provide valuable support throughout the project. Their professionalism makes them a reliable partner in clinical research.
Working with Sapientia Medicus Research has been a rewarding experience. As a CRA, I have collaborated with many SMOs, but Sapientia stands out for their proactive communication and meticulous attention to detail. Their team ensures that trials run seamlessly, with timely updates and accurate documentation. They prioritize patient safety while maintaining high recruitment numbers, which is a rare combination. I deeply appreciate their professionalism and would gladly work with them on future projects.
I had the opportunity to work closely with Sapientia Medicus Research on an Adalimumab trial, and I must commend their exceptional support throughout the process. Their team provided invaluable assistance, from patient recruitment to ensuring everything ran smoothly and efficiently. The quality of their data and their ability to meet deadlines were impressive. Sapientia's commitment to excellence and collaboration makes them a trusted partner for any clinical research project.
Working with Sapientia Medicus Research has been a great experience. Their team is proactive, organized, and highly effective in managing clinical trials. They excel in patient recruitment and consistently deliver accurate data on time. What sets them apart is their ability to anticipate challenges and address them swiftly, ensuring the success of the trials. Their professionalism and commitment to quality make them a go-to choice for any clinical research project.
