Hector Research and Archival Private Limited |  Site Management Organization (SMO)’s cover photo
Hector Research and Archival Private Limited |  Site Management Organization (SMO)

Hector Research and Archival Private Limited | Site Management Organization (SMO)

Research Services

Leading Clinical Site Management: Transforming Clinical Research Across India.

About us

HRAPL: India's Leading Site Management Organization (SMO) Specializing in Clinical Trials. Delivering Comprehensive Clinical Trial Solutions with Internationally Accredited SOPs, Our Expert Team Ensures Efficient, Compliant Clinical Trial Management Across India.

Website
https://hrapl.in/
Industry
Research Services
Company size
11-50 employees
Headquarters
Nagpur
Type
Privately Held
Specialties
End-to-end clinical site management services, Study Start-Up Services: Streamlining Clinical Trial Initiation Across India, Clinical Trial Project Management, Clinical Trial Finance Management, Advanced Clinical Trial Archival Facility, and Clinical Research Coordinator (CRC) Training Program

Locations

Employees at Hector Research and Archival Private Limited | Site Management Organization (SMO)

Updates

  • Did you know Poor data quality risks patient safety and operational efficiency? Nearly 10% of healthcare data contains defects, risking patient safety, operational efficiency, and trust in the system (Source-JAMIA). Fragmented health systems and interoperability gaps further amplify these challenges. However, strategies like Electronic Health Records (EHRs) and real-time validation have globally improved BMI reporting by 25% and childhood immunizations by 40% (Source-PubMed).

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  • Did you know? Between 2013 and 2022, the number of industry-funded oncology trials nearly doubled, and 16% incorporated patient-reported outcomes (PROs). (Source: RTI-HS)   By capturing firsthand patient insights, PROs go beyond traditional clinical measures—ensuring the patient’s voice is heard in evaluating treatment impact, quality of life, and overall trial success.

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  • Wearables in clinical trials?   Clinical trials are evolving with wearables and digital health technologies, bringing a fundamental shift in how studies are conducted. From better patient monitoring to stronger data integrity, these innovations are transforming trial efficiency.   A 2020 Tufts Center for the Study of Drug Development (Tufts CSDD) survey found that 22% of global Phase 2 and 3 trials incorporated digital health tools, including wearables. The benefits? Fewer site visits, improved efficiency, and better data collection.   Why Wearables Matter in Clinical Trials? ✅ Continuous, real-time monitoring – Wearables provide 24/7 insights into vitals, activity levels, and medication adherence, reducing dependence on-site visits. ✅ Improved patient compliance – Digital reminders, symptom tracking, and automated alerts enhance engagement and retention. ✅ Stronger data integrity – Objective, real-world evidence reduces recall bias and enhances data accuracy.   The Indian Perspective: 1. Initiatives like Ayushman Bharat Digital Mission (ABDM) are accelerating interoperability and digital adoption in healthcare. 2. More patients and researchers are embracing wearable technology, though regulatory clarity and data security remain key challenges. 3. Digital health tools reduce patient burden and expand access to clinical trials, especially in Tier 2 & 3 cities.   Wearables are not just enhancing clinical trials—they are reshaping the future of patient-centric research. As technology advances, integrating digital health solutions will be key to improving trial efficiency and patient outcomes.   What are the biggest challenges in implementing wearables in clinical trials? Drop your thoughts in the comments!

    • Benefits of using wearable devices in remote patient monitoring during clinical trials
  • Clinical Data Management (CDM) is the backbone of successful clinical trials, ensuring data quality, integrity, and compliance. From patient safety to regulatory adherence, CDM plays a vital role in advancing healthcare innovation. Key Highlights: 1. Importance of data quality and integrity 2. Strategies for protecting patient privacy 3. Emerging trends that are shaping the future of CDM Read more about it here: https://lnkd.in/gyq8XGaU #ClinicalDataManagement #ClinicalTrials  #DataIntegrity #HealthcareInnovation

    • Data Management in Clinical Trials
  • Did you know that biomarker-guided trials can reduce development costs by 20-30% and shorten timelines by 12-15 months per phase? (Source: The Oncologist Journal – PMC (PubMed Central))   Despite their proven impact, biomarkers are often dismissed as “niche tools.” In reality, they enhance treatment precision, predict patient responses, and accelerate regulatory approvals. Today, 55% of oncology trials rely on biomarker-driven designs.

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  • AI is making waves in clinical research, yet only 16% of industry leaders consider it a “top” trend in clinical trials.   Research shows AI can reduce recruitment times by 30% and cut operational delays, helping select trial sites based on data. But site selection isn’t just about numbers.   Human factors—like local community relationships, investigator engagement, patient trust, and site staff commitment—also play a crucial role.

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  • Every medical breakthrough begins with someone who cares deeply.   She notices the small details that make a big difference. She listens when others might rush. She challenges the norm by asking, "Why not?"   This International Women’s Day, we celebrate the women whose dedication strengthens healthcare and clinical research—working alongside their peers to drive progress, innovation, and compassionate care.   They bring fresh perspectives to complex challenges. They foster collaboration, ensuring every voice is heard. They remind us that behind every data point is a human story.   When diverse minds—women and men together—unite with a common purpose, clinical trials become more inclusive, treatments become more effective, and patient care transforms.   Today, we honor the incredible contributions of women in healthcare and clinical research, recognizing that true progress happens when we uplift and empower one another.   Happy International Women’s Day.   #InternationalWomensDay

    • Happy International Women’s Day
  • We are looking for a dedicated Senior Clinical Research Coordinator who is passionate about advancing clinical research and embraces a growth mindset. Our organization provides a supportive environment with comprehensive benefits and opportunities for professional development. 📍𝗟𝗼𝗰𝗮𝘁𝗶𝗼𝗻: Aligarh, Uttar Pradesh. If you are interested in joining our team, please send your resume to hr@hrapl.in.

    • Clinical Research Co-ordinator Job in Aligarh, Uttar Pradesh
  • 𝗜𝗻𝗳𝗼𝗿𝗺𝗲𝗱 𝗰𝗼𝗻𝘀𝗲𝗻𝘁 𝗳𝗼𝗿𝗺𝘀: 𝗝𝘂𝘀𝘁 𝗳𝗼𝗿𝗺𝗮𝗹𝗶𝘁𝗶𝗲𝘀? Informed consent forms are often misunderstood as tedious formalities, but they play a pivotal role in clinical trials. Far from being mere paperwork, these forms are designed to provide clear, comprehensive information about the study's purpose, potential risks, benefits, and participant rights.   These forms ensure transparency and safeguard autonomy, facilitating confident and informed decision-making. Informed consent is a crucial component that upholds ethical integrity while enabling meaningful contributions to the advancement of healthcare.

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