Carpathian Research Group
Regulatory affairs, central laboratory and clinical development services.
What they do
- Regulatory & quality
From their website
Services
- Study documentation review (opens in a new tab)
- Study materials adaptation (opens in a new tab)
- Study form development (opens in a new tab)
- Clinical project plans (opens in a new tab)
- Clinical translations (opens in a new tab)
- Investigator meetings (opens in a new tab)
- Regulatory notifications (opens in a new tab)
- Clinical study insurance (opens in a new tab)
- Investigator identification (opens in a new tab)
- Feasibility materials (opens in a new tab)
- Site selection visits (opens in a new tab)
- Site setup (opens in a new tab)
- Clinical site training (opens in a new tab)
- Site initiation visits (opens in a new tab)
- Interim monitoring visits (opens in a new tab)
- Study blinding (opens in a new tab)
- Safety event management (opens in a new tab)
- Trial Master File maintenance (opens in a new tab)
- Site audits (opens in a new tab)
- CAPA management (opens in a new tab)