In modern clinical research, the laboratory plays a critical role that goes far beyond sample analysis. It is expected to deliver accurate, traceable, and GCP-compliant data, backed by validated methods, standardized procedures, and scientific oversight.
At Diagnostiki Athinon Diagnostic Center, we approach clinical trial support with a focus on quality, scientific integrity, and operational flexibility. Our laboratory infrastructure and team are well-positioned to support pilot studies, method development protocols, and early-phase research, with a clear commitment to transparency and performance.
What Does a Clinical Laboratory Offer in a Trial Setting?
- Accurate and reproducible test results, based on validated analytical methods
- End-to-end sample traceability, from reception to reporting
- Compliance with SOPs (Standard Operating Procedures) and Good Clinical Practice (GCP)
- Production of Certificate of Analysis (CoA) and documented quality checks
- Support for method validation and custom protocol adaptation
- Direct communication with the scientific team throughout the study
Current Laboratory Capabilities
We currently support:
- Advanced biomarker testing using ELISA, qPCR, HPLC, and GC-MS
- Custom assay development or method transfer, in collaboration with the sponsor/CRO
- Sample handling (plasma, serum, DNA/RNA, stool) under controlled procedures
- Scientific documentation and result reporting suitable for research use
- Support for R&D protocols with high analytical standards and flexibility
Quality, Compliance, and Scientific Responsibility
At Athenslab, we treat each protocol as a distinct scientific collaboration. We only take on projects that match our expertise and technical infrastructure, ensuring responsibility, consistency, and data quality. Our goal is to provide precise, traceable laboratory data that support sound scientific conclusions—whether for a pilot trial, biomarker screening, or a collaborative R&D study.
