Clinical Research

NCS provides a complete offering of GCP and GLP compliant, reliable services in Phase I, II, III and IV. We have ready access to healthy normal males, postmenopausal and select patient populations. Our primary goal is collecting reliable, quality data while establishing safety and efficacy in study subjects and patients.

Our in-house quality and regulatory team ensure compliance to the protocol and ICH GCP guidelines. Our clinical support services include:

  • Feasibility Studies
  • Subject Recruitment & Planning
  • Project Management
  • Bioanalytical
  • Biostatistics
  • Scientific & Regulatory Affairs
  • Medical/Report Writing
  • PK/PD Analysis
  • Study Monitoring
Our Clinical And Bioanalytical Facilities have been inspected/audited by:

FDA, CDSCO (DCGI) India, ANVISA (Brazil), MoH (Turkey), EMA, and WHO.

Clinical Facility

  • State-of-the-art facility
  • 72 beds
  • Screening Area
  • Subject Housing Area
  • Blood Draw & Sample Processing Area
  • Dining / Recreation Area
  • 2 bed ICU
  • Deep Freezer and sample storage Area
  • Dedicated Pharmacy

147/F, 8th Main, 3rd Block,
Koramangala, Bangalore - 560034,

Studies conducted

Therapeutic Classes
  • Antibiotics
  • Anti-diabetics
  • Anti-hypertensive
  • Anti-virals
  • Anti-epileptics
  • Lipid lowering agents
  • Diuretics
  • Muscle relaxants
  • NSAIDs
  • Platelet inhibitors
  • Vasodilators
  • Phosphoiesterase inhibitors
  • Anti-Parkinson
  • Immunosuppressant
  • Anti-psychotic 
  • Corticosteroids

Clinical Trial Services Phase II, III and IV

NCS’s integrated approach to Clinical Trials ensures that sponsors benefit from the entire spectrum of services. The team is experienced in diverse therapeutic classes.

  • Cardiovascular
  • Oncology
  • Diabetes
  • Dermatology
  • Women's Health
  • Respiratory
  • Vaccine
  • Urology
  • Infectious Disease
  • Rheumatoid Arthritis
  • Nutritional Health

Integrated full service clinical trials

Pre-study Activities
  • Protocol, ICD and Trial Documents preparation
  • CRF designing and finalization
  • Regulatory Approvals/Notifications
  • Assistance with EC Dossier and Approvals
Study Conduct Activities
  • Site Training & Initiation
  • Site Monitoring
  • Project management
  • Investigation Site Training
  • Investigator Meetings and Payments
  • Quality Assurance
  • Statistical Services
Study Closure Activities
  • Query resolution
  • Database Lock
  • Site follow up
  • Site close out
  • Clinical Study Report preparation and finalization
Trials conducted in Compliance with
  • ICH GCP Guidelines
  • SOPs
  • Quality Control Checks
  • Protocol
  • Regulatory Guidelines

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