Sure.
Work with correct source data verification (SDV) and source data review (SDR).
Compliant.
Be at the cutting edge of technology with BRA framework and RBM.
Ready.
Regulation 536/2014 is coming, don't wait.
Interested?
How we can support you in GCP (Clinical Trial).
- Compliance with Regulation (EU) No 536/2014
- GCP risk management implementation/assessment
- GCP-QA Implementation/ Evaluation
- GCP Site Qualification and Training
- Data Integrity, GCP (REG 534/2014) & GCLP (EMA/INS/GCP/532137/2010) Audits
- SDV (Source Data Verification) and SDR (Source Data Review) Compliance and Data Integrity Assessment
- Inspection readiness (GCP and GCLP)
- State-of-the-Art Concepts for BRAT (Benefit-Risk Action Team) and RBM (Risk-Based Monitoring) Implementation/ Assessments
Need?
Why not book a QuickCheck?
Become part of the team.
The Entourage is looking for life science professionals.
