More than 25 years:

Your Reliable Partner for Clinical Research

The M.A.R.C.O. GmbH & Co. KG provides services for clinical trial projects for national and international pharmaceutical and biotechnology companies. We assist our partners during the entire drug/therapy development process from preclinical work to phase IV trials in the service areas presented below:

Statistics

Consultancy, Protocol Development / Sample Size Calculation, Analysis

Data Management

eCRF Application, CDISC Competency, Comprehensive Data Cleaning Process

Pharmacokinetics

Non-Compartmental Analysis (NCA), Modelling / Simulation

eSolutions

Individual Trial-related Software Solutions (e.g. eCRF, ePRO, eTMF)

Medical Writing

Trial Protocols and Reports, Investigators Brochures, Publications, Quality Control

Monitoring

On-site and Remote Monitoring

Why M.A.R.C.O.?

  • Tailored services
  • Adaptive, proactive project management
  • BfArM, EMA, FDA, WHO, PMDA experienced
  • Experienced and dedicated project teams
More about us

M.A.R.C.O. Key Figures

  • 25+ years’ experience
  • 160+ clients worldwide
  • 1700+ successfully performed projects
  • Owner-operated, flat hierarchy

Memberships

We would be happy to answer your questions about our services personally.

contact@marco-institut.de