• Training in Regulatory Affairs for Regulatory professionals (tailored to specific needs) or general for non-RA staff, Pharmacovigilance, product specific or therapy area specific for sales teams


  • Technical translations process management

Market Access Activities

  • Market access landscape activities
  • Preparation, submission and follow-up to finalisation of price and reimbursement applications, including responses to questions and support in negotiations (for selected EU countries/on-demand)
  • Pharmacotherapeutic and Economic assessment reports to support reimbursement applications (for selected EU countries/on-demand)

Scientific support

  • General literature search and compilation of scientific information as needed (on demand)

Business Development

  • Support with licensing activities