Central Laboratory

Preparation of a clinical trial is always critical. We offer a broad spectrum of services covering all aspects of the laboratory part of clinical trials – from planning to completion. Our team has considerable experience and expertise in a variety of clinical indications, their diagnosis and therapy. You have access to medical doctors, scientists, technicans and other experts for consultation.

LKF has created a sophisticated specimen retention and retrieval system, which provides comprehensive information on each sample. It ensures accurate tracking and enables instant access whenever additional or re-testing is necessary.

LKF offers a comprehensive clinical laboratory testing programme. Whenever possible, the methods and procedures applied are those recommended by international scientific societies, e.g. IFCC, ECAT, or traceable to approved reference material.

LKF provides a wide range of bioanalytical methodologies supporting all phases of the drug development process. Our highly qualified staff is experienced in the following bioanalytical areas.

Choose the parameter and time point.

The laboratory report contains the dates of specimen collection and delivery at LKF, demographic data and reference intervals. Results are flagged according to the specifications defined in the study protocol (e.g. reference ranges, alert values, exclusion/inclusion criteria).

High quality service based on the “fit-for-purpose” approach.

Our laboratory is certified according to ISO 17025 and all analytical procedures are in accordance with the relevant regulatory requirements (GCP/GLP/GMP).