Where Vision
Meets Precision

Hector Research and Archival Pvt. Ltd. (HRAPL) proudly stands as the
Site Management Organization (SMO) of choice for clinical trials in India.
Our unwavering commitment to excellence is exemplified through meti-culous adherence to the highest industry standards in every facet of trial management. At HRAPL, our comprehensive Standard Operating Procedures (SOPs) are designed to surpass stringent requirements, ensuring the seamless execution of clinical trials and instilling confidence in our clients.

With a focus on efficiency, we ensure smooth trial management, prioritizing participant safety. Committed to ethical standards, we rigorously adhere to regulations and ICH Guidelines guaranteeing data integrity and compliance. Choose HRAPL as your trusted partner for a journey marked by precision, competence, and dedication to advancing clinical research.

TRIALS IN YOUR BUDGET

Offering you multiple sites which include clinics, general hospitals, or Multi-speciality sites so that we can adjust
the study as per your budget.

COMPLETION WITHIN TIMELINES

With a large patient pool data and the number of sites,
we make sure to complete the trial within timelines.

Our History

HRAPL has started and emerged as a SMO
and we are now a pioneer into Clinical Trials.

Our Vision

Our vision is to be a preferred full-service clinical development partner and to deliver world-class services to achieve common
goals with the sponsor.

Our Mission

Our mission is encapsulated in providing a conducive system for clinical trials, in all therapy Indications, tailored to the specific requirements of the sponsor.

SERVICES

Clinical Trial Services
We do trials according to GCP guidelines in timelines and without compromising the Subject’s health.

Study Start up Services

At HRAPL, we understand the requirements of the sponsor and try to provide them

Project Management

Being in-house project managers, who are closely associated with site team.

CRC Training

At HRAPL, we are always on the lookout for talented professionals.

Archival and Management of Clinical Trial Documents

Archival Facility

HRAPL unleashes and enhances the worth of your data and resources over their.

Financial Management

100% transparent study payment transactions with the Institute, Investigator.

Expertise in handling government sites pan India

HRAPL has in-depth knowledge and experience in managing government sites addressing all their admin and logistic issues, ensuring compliance with Site SOP, GCP and all the applicable regulatory requirements.

End to end trial management at the site

HRAPL offers comprehensive trial management services, handling all aspects of clinical trials at the site. From patient recruitment and enrollment to data collection and reporting, they ensure smooth and efficient trial operations.

Efficient on-site monitoring

HRAPL excels in on-site monitoring activities, ensuring data integrity, regulatory compliance, and adherence to the study protocols. Our experienced in-house managers conduct thorough data reviews and provide real-time support to investigators and Sponsor/ CROs.

Benefits

Impactful
benefits of hiring
HRAPL brings.

On time CTMS Support

HRAPL understands the importance of a robust CTMS and provides timely support for its implementation and utilization. We ensure effective data management, tracking of trial progress, and accurate reporting through the CTMS.

Provides trained resources

HRAPL offers access to a pool of trained resources, including site coordinators, research nurses, pharmacist project managers, and other study personnel. These professionals have the necessary expertise and qualifications to support clinical trial activities effectively.

Who we are?

At HRAPL, we believe Quality + Speed of Enrolment and understand both elements are important to our clients.

HRAPL has amassed a level of expertise that enables us to:

• Manage complex across all therapeutic areas, including Neurology, Psychiatry, Oncology, Endocrinology, Cardiology, Infectious Disease, Gastroenterology, Gynaecology, Haematology, Critical Care, Paediatrics, ENT, Surgery, Orthopaedics, Nephrology, Metabolic Disease, Ophthalmology, Nutraceutical, Respiratory and other therapeutic area.

• Ensure our project team professionally executes your studies.

• Our SMO services are of the highest quality, dedicated to optimizing the management of clinical trials. We ensure seamless and efficient trial operations, contributing to the advancement of clinical research and the achievement of superior trial outcomes.