Country level
PV Support

Icon, clinical trials in central & easter europe

Cromos Pharma’s transparent and highly professional pharmacovigilance system allows us to meet our partners’ high standards. Our team provides comprehensive and flexible solutions for the active management of drug safety and risk management during the complete lifecycle of a medicinal product. We provide all the essential elements required for compliant and effective product vigilance to guarantee patient safety, including the following:


  • Therapeutic, technical, and operational excellence
  • Tailored and cost-effective safety solutions
  • Flexible outsourcing of safety functions
  • A team of QPPVs for registered products in EU
  • Up-to-date and in-depth information regarding country-specific regulatory requirements
  • Robust quality system
  • Pharmacovigilance consultancy

Cromos Pharma has over 18 years of experience in managing all aspects of clinical trials across a range of therapeutic areas. With operations in the US, Central and Eastern Europe we combine global expertise with profound local market knowledge to deliver end to end solutions supporting our pharma and biotech clients.