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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 |
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- Product Development Consulting
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- Regulatory Consulting for NCEs, INDs, NDAs
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- Clinical Trial Management (Phase I-IV)
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| Clinical Research Service |
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- Study Design
- Regulatory Consulting & Approvals
- Site Identification & Selection
- Site Monitoring
- Study Conduct & Closure
- Clinical Data Management
- Bio-Statistics
- Medical Writing Services
- Pharmacovigilance
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| For Generics |
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- Regulatory Consulting for ANDAs
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| Healthcare Services: |
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- Revenue Cycle Management
Medical Records Management
- Medical Records Management
- Claims Processing
- Healthcare Consulting
- Pharma Research & Analytics
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| Custom Staffing & Training: |
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- Karmic Clinical Academy
- Custom Staffing Solutions
- Corporate Training Services (ICH GCP, Six Sigma, CRA/CRC, Site/Investigator)
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