Clinical Research Organization Mumbai | CRO & SMO Services | Cliorbit

✨ Leading Clinical Research Excellence

Clinical Research Organization in Mumbai

Leading CRO and SMO services across Mumbai, Navi Mumbai, Thane, and surrounding areas. Expert clinical trial site management with 20,000+ sq ft research facilities and experienced investigators.

15+ Active Investigator Sites

200+ Clinical Trials Completed

5000+ Patients Recruited

25+ GCP-Certified PIs

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Mumbai Advantage

Mumbai: India's Premier Clinical Research Hub

As India's financial capital and healthcare epicenter, Mumbai offers unparalleled advantages for clinical trial execution with world-class medical infrastructure and diverse patient populations.

Why Mumbai is India's #1 Clinical Research DestinationPatient Access & Diversity20+ million metropolitan population base
Diverse demographics across socioeconomic strata
High disease prevalence across therapeutic areas
Treatment-naive patient populations

Our Locations

CliorBit Mumbai Operations

Comprehensive clinical research coverage across Greater Mumbai region

South Mumbai

Premium hospital sites in Worli, Mahim, Lower Parel with specialty departments

Central Mumbai

Andheri, Bandra, Kurla - High patient volume sites with multi-specialty coverage

Navi Mumbai

State-of-the-art facilities in Vashi, Nerul, Kharghar with modern infrastructure

Thane & Extended Suburbs

Growing network in Thane, Kalyan, Dombivli for wider patient reach

Our Services

Specialized Clinical Trial Services

Site Management Organization (SMO)

Complete end-to-end site-level operations and coordination

Site identification and feasibility across Mumbai region
Investigator site activation and training
On-site clinical research coordinator placement
Real-time monitoring and quality oversight
Protocol compliance management
Site close-out and archival services

Patient Recruitment Mumbai

Strategic multi-channel recruitment leveraging Mumbai's population

Hospital outpatient department (OPD) recruitment
Community healthcare center partnerships
Digital recruitment campaigns (Mumbai-targeted)
Patient database access across therapeutic areas
Pre-screening and eligibility assessment
Retention strategies and follow-up coordination

Nutraceutical & Supplement Trials

Specialized expertise in nutrition and wellness product research

FSSAI-compliant nutraceutical study design
Protein efficacy and bioavailability studies
Supplement safety and tolerability trials
Ayurvedic and herbal product evaluation
Sports nutrition clinical research
Functional food ingredient testing

Clinical Trial Monitoring

Rigorous quality assurance and data integrity

On-site monitoring visits (Mumbai sites)
Source data verification (SDV)
Protocol deviation management
Safety reporting and pharmacovigilance
Regulatory inspection readiness
Audit support and CAPA implementation

🔬 Therapeutic Areas

Therapeutic Expertise in Mumbai

Experienced principal investigators across diverse therapeutic areas

Oncology Clinical Trials

Access to Tata Memorial Centre and leading cancer hospitals with experienced oncology investigators for Phase II-IV trials

Cardiology & Metabolic Studies

Extensive experience in cardiovascular, diabetes, and metabolic disorder trials with high patient prevalence

Gastroenterology Research

Specialized GI investigators at premier hospitals for IBD, GERD, and liver disease studies

Respiratory & Infectious Disease

Strong infectious disease infrastructure and respiratory medicine expertise with NABL-certified microbiology labs

Nephrology & Urology

Leading nephrologists and dialysis centers for renal disease and transplant studies

Neurology & Psychiatry

Comprehensive neuroscience research capabilities with behavioral health assessment facilities

Compliance & Quality

Regulatory Excellence in Mumbai

Mumbai's Regulatory Ecosystem Advantage DCGI Regional Office Proximity: Direct access to Drug Controller General of India (DCGI) Mumbai office for faster regulatory clearances and queries
 Institutional Ethics Committees (IEC): Multiple CDSCO-registered ethics committees with rapid review timelines (14-21 days average)
 NABL-Accredited Labs: Over 20 NABL-accredited clinical laboratories in Mumbai for protocol-compliant sample analysis
 Central Licensing Authority: Maharashtra FDA office in Mumbai for state-level regulatory coordination
 GCP Training Centers: Regular Good Clinical Practice training programs conducted by Mumbai-based organizations

Regulatory Services

Ethics committee application and submission
DCGI clinical trial application (Form-44)
Import license coordination for investigational products
CTRI (Clinical Trials Registry - India) registration
SAE reporting to regulatory authorities
Regulatory inspection support

Quality Assurance

ISO 9001:2015 certified operations
ICH-GCP compliant SOPs
Internal quality audits
Investigator site qualification visits
Training and certification programs
CAPA management systems

Why Choose Us

Why Sponsors Choose CliorBit Mumbai

40% Faster Study Start-Up

Pre-qualified investigator network and streamlined ethics submissions reduce Mumbai site activation time from 12 weeks to 7-8 weeks average

Superior Recruitment Rates

Average enrollment rate 30% higher than national average leveraging Mumbai's 20M+ population and established patient databases

Zero Critical Audit Findings

100% audit success rate across 50+ sponsor audits and regulatory inspections at Mumbai sites over past 3 years

Experienced Investigator Network

25+ GCP-certified principal investigators with average 10+ years clinical trial experience across 15+ therapeutic areas

Start Your Clinical Trial in Mumbai

Partner with Mumbai's most experienced clinical research organization for your next study

Contact Mumbai Team

Connect@cliorbit.com | +918767307223 | Mumbai, Maharashtra