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Choosing an appropriate partner for your drug development process is the most critical step in Clinical Research. FCRL provide innovative, effective and most comprehensive research services for your Clinical Trails needs through its association with highly experienced Investigators belonging to Fortis Hospital network.
FCRL provides full range of services for Phase I in healthy volunteers (NMEs and generic products), Phase I in oncology, Phase II – IV in patients as well as bioequivalence studies in healthy volunteers and patients.
Full Spectrum of Clinical Research Services are provided by FCRL under one roof :
- Early Clinical Drug Development
BA/BE studies: Clinical, Bioanalytical section
List of Assays/List of Validated Methods
Phase I / First in man administration studies
- Phase II to Phase IV Clinical Trials
Capabilities/Experience in Phase II – IV
Therapeutic Expertise
- Feasibility and Site Selection
- Project Management
- Clinical Monitoring
- Regulatory Services
- Clinical Data Management
- Medical Writing
- Medical Monitoring
- Site Management
- Central Laboratory
- Central Pharmacy
- Quality Assurance and Training Services
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