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Clinical Trial Management
  • Karmic has a robust Pan-India network of over 500+ qualified sites, 1000+ Investigators and an overall monthly patient load of 10,000+ patients across multiple therapeutic areas.
  • Our Site network includes General Hospitals, Super Specialty Hospitals and Private Clinics on a pan-India basis across key cities including Mumbai, Pune, Bangalore, Delhi, Chennai, Ahmedabad, Nasik, Bhopal, Patna, Kolkata, Cochin, Coimbatore, Hyderabad, Indore and other tier 2 cities.
  • ICH-GCP/E6 trained Clinical Operations team Project Managers, Team Leaders ,Clinical Research Associates(CRAs) and Clinical Research Consultants CRCs with 2-8 years of field experience across key therapeutic segments.
  • Independent Medical Monitors with modern medicine (MBBS) degrees deputed on key clinical projects.
  • Independent Quality Assurance function reporting directly to CEO. Quality assurance at sites managed by CRCs and independent site auditors.
  • Comprehensive set of over 30 ICH-GCP based SOPs to cover all aspects of clinical operations.
  • Flexible in-sourcing of CRAs on a long-term and short-term basis.
k-Trials™

Our Proprietary Trial Management Methodology which combines a CRO model with an SMO model and thereby provides strong Site Monitoring & Trial Conduct capabilities alongwith rapid Site Identification, Feasibility and Initiation. We further leverage Remote Monitoring capabilities for early query resolution, site clarification management and significant reduction in physical site monitoring costs. The diagram below gives an overview of our methodology:

k-Trials: Our Proprietary Trial Management Methodology
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