MBR Consulting S.C. – your partner in Clinical Trials

We can support your Team in various  activities as:

• Feasibility studies

• Complete Clinical Trials Application (CTA) service (preparation and submission)

• Monitoring Phase II to IV trials (All studies are run to GCP/ICH standard)

• Phase I, bioequivalence studies   (GCP/ICH standard)

• Study Protocol, CRF preparation

• Study Regulatory Approval

• GCP training for Investigators