Pepgra
Regulatory affairs, clinical data management and clinical development services.
What they do
- Regulatory & quality
From their website
Sub services
- Clinical Trial Audit and Monitoring Services (opens in a new tab)
- Clinical Study Design (opens in a new tab)
- Global Regulatory & Clinical Writing Services (opens in a new tab)
- Clinical Biostatistics & Statistical Programming (opens in a new tab)
- Clinical Trial Patient Recruitment (opens in a new tab)
- Post-Market Surveillance (opens in a new tab)
- Clinical Technology & Process (opens in a new tab)
- Clinical Study Protocols (opens in a new tab)
- Full Dossier Development (opens in a new tab)
- Regulatory eCTD dossier preparation (opens in a new tab)
- Clinical Evaluation Reports (opens in a new tab)
- Case/Exposure Management (opens in a new tab)
- Adverse Event Follow Up (opens in a new tab)
- Post-marketing Literature Surveillance (opens in a new tab)
- Complaint management (opens in a new tab)
Show all (41)
Sub services
- Adaptive Design Clinical Trial (opens in a new tab)
- Randomization (opens in a new tab)
- Interim analysis (opens in a new tab)
- Blinding (opens in a new tab)
- Parallel Group Design (opens in a new tab)
- Cross over design (opens in a new tab)
- Intent-to-treat (ITT) analysis (opens in a new tab)
- SAS (opens in a new tab)
- R (opens in a new tab)
- Cdisc SDTM (opens in a new tab)
- Patient recruitment globally (opens in a new tab)
- Cloud-based Patient identification (opens in a new tab)
- Multilingual support (opens in a new tab)
- EDC, CTMS, eTMF platforms (opens in a new tab)
- Site assessment (opens in a new tab)
- Custom software images (opens in a new tab)