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Product Development Clinical and Regulatory

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

VPA 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.

Meet our practice leads