Accreditation

To ensure accurate, reliable, and timely results, we follow strict quality standards. Accredited under both German (DAkkS) and international (CAP/CLIA) guidelines, we maintain the highest operational quality, with our analyses recognized worldwide, including in the U.S. Our successful accreditations under DIN EN ISO 15189 and DIN EN ISO/IEC 17025 demonstrate our commitment to high-quality standards and expertise.

Quality control and Proficiency testing

Internal quality assurance is conducted according to the guidelines of the German Medical Association (Bundesärztekammer). Additionally, for testing procedures not covered by the RiliBÄK guidelines, equally strict quality requirements are implemented. External quality assurance is ensured through regular participation in proficiency testing programs.

For more information on our proficiency testing program, please get in touch.

Project Management /clinical trail services

  • Planning new projects

    If you have an upcoming project, don’t hesitate to reach out to us. With our extensive knowledge of the laboratory's capabilities and a clear understanding of your specific requirements, we can establish an early timeline and plan to ensure the smooth and efficient progression of your project. We are committed to supporting you every step of the way, offering expert advice and reliable service to meet your needs..

  • Providing logistical support

    We collaborate with trusted logistics partners to assist with your sample transportation needs. We can guide you through the process, ensuring that your samples are handled efficiently and safely.

    Additionally, we provide detailed instructions regarding preanalytic procedures and temperature requirements during transport, ensuring that samples are preserved in optimal conditions throughout their journey. Our team is here to support you, ensuring that your logistics are managed smoothly and in compliance with all necessary guidelines.

  • Data Management

    Our Quality Management (QM) department is dedicated to providing all the necessary documentation required by regulatory bodies for your project. We understand the importance of compliance, specifically GMP guidelines, and our team ensures that all relevant paperwork is accurately prepared and up-to-date.

    Throughout the course of the project, we hold regular meetings to discuss and address any document requirements you may have, ensuring that everything is in line with regulatory standards. Our proactive approach helps streamline the process and keeps your project on track, giving you peace of mind that all necessary documentation is handled efficiently and professionally.

  • Customer audits

    Customer audits are an essential part of maintaining transparency and trust. Our Quality Management (QM) department will handle the scheduling process, ensuring that the audit is conducted at a convenient time and in accordance with your specific requirements.

    We recognize the importance of these audits in upholding transparency, trust, and regulatory compliance. Our team is committed to making the process smooth and efficient. Whether your audit is for compliance, quality assurance, or any other purpose, our QM department will provide comprehensive support, ensuring all necessary resources and personnel are available to facilitate a successful audit.

Get in touch with us today.

Your trusted lab in Europe.