CLINICAL RESEARCH SERVICES
ANVI CONSULTING manages clinical trials from Phase I through Phase IV. We handle the study design, site management, patient enrollment, data collection, and regulatory paperwork.
We run clinical trials for drug companies.
How We Run Trials
Trial Design : Real-world protocols with flexible scheduling and remote monitoring options. Designed for patients to actually complete the study.
Data Quality : Risk-based monitoring and source verification. ICH-GCP compliant throughout.
Regulatory Knowledge : Former FDA/EMA staff who know what regulators want. Right documentation from day one.
What We Handle
Early Phase Studies
- First-in-human safety studies
- Dose escalation and PK
- Drug interaction studies
Late Phase Studies
- Registration trials for approval
- Long-term safety studies
- Post-market real-world data
Clinical Operations
- Site identification and vetting
- Patient recruitment and retention
- Site monitoring and safety reporting
Data Management & Statistics
- Electronic data capture setup
- Database validation and cleaning
- Statistical analysis and reports