Experience in real-world studies and registry research.
3P Consulting GmbH supports the planning, implementation and scientific use of non-interventional studies, registries, post-authorisation studies and publication-driven real-world evidence projects.
The scientific leadership and associated expert network bring extensive experience from long-term disease registries, sponsor-supported observational studies, investigator-initiated research and post-authorisation research across several therapeutic areas.
Project-specific references are provided where publicly disclosed or with appropriate permission.
Design, protocol development, CRF/eCRF concepts, site documentation, safety interfaces, data-management coordination and study reporting for observational research.
Registry strategy, longitudinal data capture, follow-up concepts, centre engagement, plausibility checks, analysis planning and scientific output.
Support for academic study concepts, ethics-facing documentation, publication strategy, abstracts, manuscripts and congress deliverables.
Analysis concepts, endpoint definition, interpretation of registry data, medical writing and coordination of multi-author scientific outputs.
Therapeutic areas include pulmonology, interstitial lung disease, pulmonary hypertension, rheumatology, immunology, cardiovascular medicine, growth hormone treatment and selected rare diseases.
Detailed project references, therapeutic-area examples and sponsor-facing case descriptions can be provided in a project-specific context, subject to confidentiality and prior permissions.