We can help your business to:
- Design clinical studies from concept through to full protocol
- Run / outsource clinical trial project management and delivery
- Analyse and report from clinical studies
- Achieve routine compliance with GLP/GCP
- Build high-quality regulatory documentation, supporting CTA, MAA and device submissions
Phetairos Product Development – Clinical and Regulatory Services (PDCR) is a group of leading industry subject matter experts with a proven and well-established record of achievement across all phases of drug development in a broad range of therapeutic areas. We have a passion for clinical development and mastery of local and global regulatory issues, landscapes and guidelines.