Your High-Enrolling Clinical Research Partner in India

India Clinical Research Partner

Designed for high-enrollment studies requiring speed, scale, and predictable execution. Backed by the SRM Group, a $1.4B+ leader in hospital systems and education.

500,000+

Patients Annually

400+

Clinical Sites

800+

Clinicians

15+

Years Experience

Built for Speed, Scale, and Quality

InoRx integrates embedded investigators, clinical sites, and direct patient access within the SRM hospital ecosystem — resulting in faster enrollment, stronger retention, and more predictable execution.

Faster Study Start & Enrollment

Embedded hospital infrastructure enables rapid site activation and patient recruitment without external site dependency.

High-Enrollment Execution Model

Direct access to large pre-existing patient populations supports consistent enrollment across Phase I–IV programs.

Quality Without Tradeoffs

ICMR-certified environment with established clinical, safety, and regulatory processes. Audit-ready data aligned with global standards.

Proven in High-Volume Settings

15+ years of execution within the SRM hospital network, with global CRO collaboration including IQVIA.

Deep Expertise Across Key Therapeutic Areas

Supported by high-volume patient populations and integrated clinical environments within the SRM network.

Infectious Diseases & Vaccines

Rapid enrollment in acute care settings

Respiratory & Pulmonary

Asthma, COPD, and infectious respiratory studies

Inflammatory & Immune Conditions

Longitudinal cohorts and chronic disease access

Dermatology

Access to diverse patient populations

Biosimilars & Generics (SMD)

Bioequivalence and PK/PD execution

Cardiometabolic

Diabetes and cardiovascular outcomes

Oncology

Biosimilar programs with long-term follow-up

Women's & Neonatal Health

Peri/post-partum, neonatal, OB/GYN populations

Supporting Every Phase of Development

From first-in-human studies to large-scale post-marketing registries, InoRx delivers across the full clinical development spectrum.

First-in-Human

Phase 1a/1b, disease-agnostic studies. 20-bed unit operational today, expandable to 30–50 beds within 1–2 months.

Large-Scale & Real-World

Disease-focused and registrational programs with rapid recruitment across 400+ sites and 500,000+ annual patient touchpoints.

Fast, High-Volume 
Enrollment

PK/PD, bioequivalence, post-marketing surveillance, and real-world evidence with compliant long-term follow-up.

Clinical Infrastructure & Patient Access

InoRx operates an integrated site and hospital infrastructure enabling rapid capacity scaling without external site dependency.

Clinical & Laboratory Capabilities

Patient Access & Site Network

End-to-End Clinical Development Support

Full-service capabilities from trial design through regulatory submission and post-market surveillance.

Trial Design & Feasibility

Protocol optimization for high-enrollment settings

Clinical Operations & Monitoring

On-site and remote monitoring capabilities

Data Management & Analysis

Statistical support and audit-ready datasets

Regulatory Submission Support

ICMR and global regulatory processes

Safety & Pharmacovigilance

Structured safety reporting and monitoring

Biosimilar Development

Phase II–III registrational trial support

Generics (SMD) & Bioequivalence

High-volume BE study execution

Phase IV & Real-World Evidence

Post-marketing and registry programs

Partner with InoRx in India

Ready to accelerate your clinical program? Contact us to discuss feasibility, site capabilities, and how InoRx can meet your enrollment goals.