Aml Research

Clinical Trial Monitoring

Monitoring is a crucial aspect in clinical trials and garantuees subject’s rights and welfare and data integrity.  At AML we understand the importance of monitoring for the success of a clinical trial.

Our skilled, multi-langual and well-trained  Clinical Research Associates (CRAs) ensure the highest quality review of data and make up an effective line of communication with the trial sites.

Our Clinical trial Monitoring services include:

  • Research Site selection and pre-study assessments
  • Site selection, study start-up and initiation
  • Competent Authorities and Ethics Committees submissions & communication
  • Contract/ Clinical Trial Agreement (CTA) negotiations
  • Routine monitoring ( remote monitoring, on-site monitoring visits, risk-based monitoring)
  • Close-out visits
  • Secondary monitoring

 

AML’s clinical research operational services are available within Belgium, The Netherlands and Luxembourg. We specialized our services to this region to ensure full knowledge of local regulations, culture, healthcare structures and for most responsive coverage.

For the monitoring in other European countries, we can rely on a network of experienced partner CROs.