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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
- Regulatory Consulting for NCEs, INDs, NDAs
- Clinical Trial Management (Phase I-IV)
- Clinical Data Management
- Pharmacovigilance
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| For Generics |
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- Regulatory Consulting for ANDAs
- Bio-Equivalence Studies
- Bio-Availability Studies
- Post Marketing Studies
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| Clinical Services |
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- 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
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