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Karmic Lifesciences – your services partner for comprehensive drug development services out of India – combines a highly experienced medical team with deep therapeutic expertise, a prolific network of pan India sites and investigators, a fully CFR Part 11 compliant technology infrastructure and a strong culture of client responsiveness to significantly speed up your clinical trials while ensuring strict adherence to ICH-GCP standards and trial budgets.

We provide a comprehensive range of services, directly and through our strategic partners to encompass Clinical Trial Management, Clinical Data Management, Bio-Statistics, Medical Writing, Regulatory Consulting, Drug Safety & Pharmacovigilance and Bio-Analytical Services across Early to Late Phase (Phase I through IV) and Pre-Clinical Research.
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For Innovators
  • Product Development Consulting
  • Regulatory Consulting for NCEs, INDs, NDAs
  • Clinical Trial Management (Phase I-IV)
  • Clinical Data Management
  • Pharmacovigilance
For Generics
  • Regulatory Consulting for ANDAs
  • Bio-Equivalence Studies
  • Bio-Availability Studies
  • Post Marketing Studies
Clinical Services
  • Study Design
  • Regulatory Approvals
  • Investigator Recruitment
  • Investigator Training
  • Patient Recruitment
  • Medical Monitoring
  • Study Conduct & Close-out
  • Data Management
  • Bio-Statistics
  • Medical Writing
  • Pharmacovigilance
  • Central Lab Services
  • Core ECG Services
  • Quality Assurance