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Why Argentina

Rationale of Conducting Clinical Trials in Argentina

Highly profesional and motivated investigators

  • Evidence for qualification available from up-to-date participation in multi-center clinical trials
  • Participation in clinical studies considered honorable and prestigious
  • Contribution to the world science - acknowledgment for professional skills
  • Exchange of clinical and scientific experience
  • Investments in healthcare system
  • Personal economical benefits

Time saving

  • National approval obtained within 3 month!
  • Fast patient recruitment
  • Smooth Import Procedure

Large number of patients

  • Wide access to all patient populations
  • drug -naive population to certain medications (oncology treatment, asthma inhalers)

Reliable documentation

  • Coherence between Source Documentation and Case Report Forms
  • Adequate data flow within required time frames
  • Potential for immediate resolving of each query
  • Very few to none lost-to-follow-up patients

Strict regulatory control

  • Primary control, performed by Independent Ethic Committee
  • ANMAT conducts audits and inspections at sites, Ethics Committees and CRO offices under GCP and local requirements
  • Routine auditing on international level

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