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16 – 29 Nov 2026 | Düsseldorf, Germany

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M.A.R.C.O. GmbH & Co. KG - Institute for Clinical Research and Statistics

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www.marco-institut.de/Düsseldorf, Germany
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About

Since nearly 30 years, the M.A.R.C.O. GmbH & Co. KG provides services for clinical trial projects for national and international medical device, pharmaceutical and biotechnology companies. We assist our partners during the entire device/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 ProcesPharmacokinetics

  • 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

  • Pharmacokinetics

    Non-Compartmental Analysis (NCA), Modelling / Simulation

E-HEALTH

Safety & systemsSensors & Wireless productsHealth information managementRemote diagnostics

MEDICINE

Biostatistics, EpidemiologyClinical Research, Trials

THERAPEUTIC AREA

Cardiology/Vascular DiseasesDental & Oral HealthDermatologyDiagnosticsEndocrinologyGastroenterologyGenetic DiseaseHematologyHepatologyImmunologyInfections and Infectious DiseasesInternal MedicineMusculoskeletalNephrologyNeurologyNutrition and Weight LossObstetrics/GynecologyOncologyOphthalmologyOrthopedics/Orthopedic SurgeryOtolaryngologyPediatrics/NeonatologyPharmacology/ToxicologyPodiatryPsychiatry/PsychologyPulmonary/Respiratory DiseasesRare DiseaseRheumatologyTraumaUrologyVaccines

VALUE CHAIN

Auditing & AnalyzingDesign / R&D / EngineeringSoftware & App Development

Representatives

Executive Assistant ǀ Client Manager ǀ Medical Writer

M.A.R.C.O. GmbH & Co. KG - Institute for Clinical Research and Statistics

Marketplace (6)

  • Service

    Statistical Consultancy / Planning / Analysis for Clinical Trials

    Based on our fundamental knowledge and the experience of our statistic experts, we offer statistical consultancy, planning, analysis and reporting for clinical trials.

    • Consulting
    Author

    Executive Assistant ǀ Client Manager ǀ Medical Writer at M.A.R.C.O. GmbH & Co. KG - Institute for Clinical Research and Statistics

    Düsseldorf, Germany

  • Service

    Data Management for Clinical Trials

    Our experienced data managers work with our in-house EDC System /eCRF and have a comprehensive data cleaning procedure in place to improves communication between the Sponsor and the executing parties and to support the Sponsor’s oversight in a study.

    Author

    Executive Assistant ǀ Client Manager ǀ Medical Writer at M.A.R.C.O. GmbH & Co. KG - Institute for Clinical Research and Statistics

    Düsseldorf, Germany

  • Service

    Pharmacokinetic Analysis for Clinical Trials

    Pharmacokinetics (PK) and Pharmacodynamics (PD) are essential aspects when new compounds or drugs are tested. Pharmacokinetics describes what the body does with the substance including ADME processes (Absorption, Distribution, Metabolism, Excretion).

    Author

    Executive Assistant ǀ Client Manager ǀ Medical Writer at M.A.R.C.O. GmbH & Co. KG - Institute for Clinical Research and Statistics

    Düsseldorf, Germany

  • Service

    eCRF / EDC System for Clinical Research: Data and Trial Management

    We offer clinical trial-related software solutions and appendant application services.

    Author

    Executive Assistant ǀ Client Manager ǀ Medical Writer at M.A.R.C.O. GmbH & Co. KG - Institute for Clinical Research and Statistics

    Düsseldorf, Germany

  • Service

    Medical Writing for Clinical Trials and Publications

    Based on our great expertise, we offer medical writing services for all documents relvant for clinical trials.

    Author

    Executive Assistant ǀ Client Manager ǀ Medical Writer at M.A.R.C.O. GmbH & Co. KG - Institute for Clinical Research and Statistics

    Düsseldorf, Germany

  • Service

    eConsent Tool for Non-Interventional Studies

    The eConsent functionality enables study participants to review and electronically sign the informed consent within the eCRF environment.

    Author

    Executive Assistant ǀ Client Manager ǀ Medical Writer at M.A.R.C.O. GmbH & Co. KG - Institute for Clinical Research and Statistics

    Düsseldorf, Germany