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We have a highly skilled team with many years of experience in the field of unicentre and multicentre trials, national and international, in any of clinical trial phases (Phase I to Phase IV).

  • PREPARATION OF INVESTIGATIONAL MEDICINAL PRODUCT Dossiers (IMPD) and CLINICAL TRIAL APPLICATIONS:
    • Ethical Committees.
    • Spanish Drug Agency.
  • STUDY DESIGN AND PREPARATION OF PROTOCOLS.
  • MONITORING OF CLINICAL TRIALS by highly qualified staff.
  • PREPARATION AND REVIEW OF SOPs for the monitoring of clinical trials according to GCP guidelines.
  • SPECIALISED TECHNICAL CONSULTANCY covering all items concerning Phase I, II, III and IV clinical trials related to:
    • Spanish, European Union and USA regulations.
    • Research centres and investigators.
  • TRAINING OF MONITORS to ensure that clinical trials are performed according to GCP.
  • WRITING OF FINAL AND INTERIM REPORTS.
  • WRITING OF PUBLICATIONS, POSTERS AND PRESENTATIONS TO CONGRESSES, including translations to any language required.
  • SPECIALISED TECHNICAL TRANSLATIONS of protocols, investigator brochure, CRF, etc.

Our experience includes:

  • Hepatic and renal transplant.
  • HIV.
  • Vascular neurology.
  • Cardiovascular.
  • Gastroenterology.
  • Rheumatology.
  • Microbiology.
  • Dermatology.
  • Alzheimer’s disease.
  • Immunology.

ÁGORA FARMACÉUTICA, S.L.
c/ Juan Hurtado de Mendoza nº 9 - 809 . Madrid 28036. España. • Tel: +34 91 359 30 79. Fax: +34 91 345 25 18
agora@agorafarmaceutica.com