Clinical Research & Operations (CRO Services) – IJCP Group
IJCP Group offers integrated and compliant Clinical Research Organisation (CRO) Services along with advanced Clinical Research and Operations (CRO) services in India, South-East Asia and the GCC region. Our team supports pharmaceutical companies, medical device manufacturers, biotech innovators, and global health organisations with end-to-end clinical trial planning, execution and real-world evidence support.
With CRO registration underway, IJCP is equipped to deliver scalable, fast and high-quality clinical research, supported by India's largest network of healthcare professionals and strong regional partnerships across Asia.
500,000+
Healthcare Professionals
Multi-Region
India, SEA & GCC
Phase III-IV
Clinical Trials
ICH-GCP
Compliant
Why IJCP for Clinical Research?
Rapid Large-Scale Patient Recruitment
Through IJCP's network of 500,000+ healthcare professionals
Integrated CRO and Real-World Evidence (RWE) Expertise
Comprehensive support across all research phases
Strong Therapeutic Experience
Across metabolic disorders, endocrinology, cardiology, paediatrics, women's health, respiratory and infectious diseases
Deep Understanding of Regulatory Pathways
India, SEA and GCC regulatory expertise
Strong Presence Across Cities
In tier I, II and III cities for faster site activation and study enrolment
Technology-Driven Operations
With EDC, eCRF and remote monitoring capabilities
Our Clinical Research & Operations Capabilities
Comprehensive end-to-end CRO services supporting pharmaceutical, biotech, and medical device innovators
Protocol Development & Scientific Consulting
- Study protocol design aligned with global regulatory expectations
- Scientific and medical consulting from subject-matter experts
- Feasibility assessment and risk-based planning
Site Feasibility & Selection
- Data-driven feasibility with real-time access to multi-specialty clinicians
- Selection of high-performing investigators and accredited clinical sites
- Startup support for rapid site activation
Clinical Monitoring (On-site & Remote)
- Qualified CRAs for GCP-compliant monitoring
- Remote, hybrid and risk-based monitoring frameworks
- Continuous oversight for patient safety and protocol adherence
Phase III–IV & Observational Study Operations
- Multicentric Phase III & IV trial management
- Observational, post-marketing surveillance and epidemiology studies
- Seamless coordination with investigators, CRO teams and sponsors
Data Management, EDC Setup & Biostatistics
- EDC platform setup, eCRF design and validation
- Data cleaning, query resolution and statistical programming
- Biostatistical analysis and study reporting
Pharmacovigilance (PV) Support
- AE/SAE collection, reporting and documentation
- Safety data management for interventional and observational studies
- Compliance with local and international PV regulations
Regulatory Submissions (India, GCC & SEA)
- Preparation and submission of regulatory dossiers
- Coordination with CDSCO, ethics committees and regional authorities
- Guidance on country-specific compliance requirements
Ethics Committee (EC) Coordination
- EC submission and approval management
- Rapid turnaround through established EC networks
- Ongoing compliance monitoring
Patient Recruitment & Engagement
- Access to IJCP's extensive healthcare provider and specialty networks
- Strong outreach in urban and semi-urban locations
- Ethical patient communication and high retention rates
Therapeutic Expertise
IJCP supports clinical studies across major therapeutic areas, including:
Metabolic and Endocrine Disorders
Cardiology and Cardiovascular Research
Paediatrics and Neonatology
Women's Health and Reproductive Medicine
Respiratory, Infectious Diseases and Immunology
Oncology (Non-interventional and Observational)
Rare Diseases (Feasibility-based)
Our Strengths
Fast Recruitment Across India & Asia
Access to a wide clinical ecosystem ensures reliable and accelerated study enrolment.
Integrated CRO + RWE Capabilities
End-to-end support from controlled trials to real-world evidence, HEOR, and post-marketing research.
Strong Multiregional Coverage
Presence across India, Southeast Asia, and the GCC, enabling region-wide study expansion.
Compliance-Driven Operations
All studies follow ICH-GCP, local ethics guidelines, and global regulatory standards.
Partner With IJCP Group
IJCP Group combines scientific expertise, regional reach and robust operational capabilities to help life sciences organisations conduct high-quality, compliant and timely clinical research.
Contact us to discuss your Clinical Research requirements and explore collaboration opportunities.
Contact UsIJCP Group supports healthcare organisations across Asia, the Middle East, and emerging global markets through evidence-based communication, education, and publishing solutions.
