Late Stage Development
Innovative tools like the fully validated AMS BYOD-type Patient Reported Outcome solution (AMS ePro®) will help to save money and time, e.g. with Patient Diaries and Quality of Life Questionnaires.
AMS has extensive experience in Late-phase studies (Phases IIIb and IV) and is prepared for the quite new concept of Low-intervention Clinical Trials. The challenge of high-quality data while meeting all requirements, tight timelines and a limited budget, remains in Non-interventional studies (NIS).
In a non-interventional study, you may want to collect Real World Evidence Data and include a large number of investigators and institutions – AMS processes ensure a smooth handling of all study activities.
Although your project plan is easy, compliance may be problematic. AMS staff are aware of regulatory and data protection requirements and assure compliance during the course of your study.
Read more or find out how AMS Clinical Research services can meet your needs:
Get in touch with us at: Research@ams-europe.com