Clinical Trial Site Management

Advancing Clinical
Research Excellence

Full-service SMO providing comprehensive administrative, regulatory, and operational support for Phase II–IV clinical trials with unwavering commitment to ethics and ICH-GCP compliance.

Phase II–IV
Trial Support
13+
Therapeutic Areas
ICH-GCP
Compliant
Who We Are

Quality, Ethics &
Compliance First

Clinex Research Service is a Clinical Trial Site Management Organization based in Belagavi, India. We provide comprehensive administrative, regulatory, and operational support to clinical trial sites—helping investigators conduct ethical, compliant, and high-quality research.

Our team of experienced Clinical Research Coordinators (CRCs) work onsite to reduce clinical staff workload, improve trial quality, and ensure every patient is recruited and managed in strict accordance with protocol and site requirements.

Onsite CRCs

Experienced coordinators deployed directly to your institution

ICH-GCP

Every process aligned with international compliance standards

Site Preparation

End-to-end clinical trial site readiness and setup

Risk Management

Proactive compliance risk identification and mitigation

What We Offer

Comprehensive SMO Services

Streamlining clinical trial operations from site preparation through regulatory compliance and patient management.

CRC Services

  • Patient eligibility screening & support
  • Informed consent process management
  • Patient visit & follow-up scheduling
  • Clinical trial material management
  • CRF / eCRF preparation support
  • Clinical Research Associate support
  • Audit & regulatory inspection readiness

Site Administration

  • Clinical trial site preparation
  • IEC/IRB submission & coordination
  • Trial document preparation & management
  • Invoice & financial documentation
  • Regulatory inspection support
  • Medical institution identification
  • ICH-GCP aligned documentation

Regulatory & Contracts

  • Clinical trial contract management
  • Clinical trial initiation requests
  • Essential document maintenance
  • IEC/IRB arrangement & review
  • Invoice management
  • Compliance risk management
  • Protocol compliance oversight
Areas of Focus

Deep Therapeutic Expertise

General MedicineGastroenterologyUrologySurgeryOrthopaedicsOphthalmologyGynaecologyPulmonaryNeurologyPsychiatryPaediatricsDermatologyENT

Therapeutic Breadth

Experienced research professionals across 13+ therapeutic areas, ensuring quality data collection and regulatory compliance at every stage.

Clinical Sites

We support clinical trials at both government and private medical institutions, adapting our services to each site's unique operational needs.

Laboratory Services

Collaboration with NABL-accredited laboratories for pathology and radiology investigations, aligned with protocol requirements.

Get Started

Let's Work Together

Ready to streamline your clinical trial operations? Reach out and let's discuss how Clinex can support your research goals.

Managing Director
Mr. Sudhir Shende
Location
Belagavi, Karnataka, India
Send an Email