Pharmacovigilance of clinical trials Print E-mail
  • Comprehensive Management of Adverse Eventsensayos_clinicos
  • Database Design for the management of Adverse EventsData Encryption
  • Preparation of Safety Annual Reports and DSURs (updated to the current law)
  • Preparation of Standard Operating Procedures in Clinical Trials Pharmacovigilance
  • Design of Informed consent documentation and Case Report Forms
  • Processing of permits with Regulatory Agencies (AEMPS), Ethics Committes, Local Authorities
  • Monitoring
  • Consultancy