Reliable data for your research – even with small sample volumes
Contract Analytical Testing & Applications with TRIGA-S
Our expert team in the biosafety level 2 (BSL-2) laboratory supports you with precise contract testing, robust method comparisons, and meaningful feasibility analyses. We combine state-of-the-art automated platforms with manual precision to find the right solution for every IVD study and every contract testing project – flexible, fast, and with no minimum order quantities.
All our services can be booked individually or as a complete package – precisely according to your needs.
Safety and Efficiency for Your Project
Maximum Precision
Reliable results even with small sample volumes. Our optimised methods conserve your valuable sample material and deliver precise data.
Quick Start
With no minimum order quantities and with focused pilot projects, we allow you to test hypotheses rapidly and minimize risks before investing in larger studies.
Audit-ready Quality
We are ISO 13485-certified, deliver validated methods, complete documentation, and audit-ready reports – ready for Notified Bodies and competent authorities.
Maximum Flexibility
Whether automated analysis or manual fine-tuning for demanding matrices and special samples – we adapt our processes to your requirements.
Uncompromising Safety
We work in a BSL-2 laboratory, and our ISO 13485-compliant processes ensure industry-standard practices for the safe handling of all materials.
Innovation and Decision-Ready Expertise
Our method comparisons and feasibility analyses provide clear, decision-ready evidence for platform selection and assay design decisions.
Our services in detail
Contract Analytical Testing & Applications
All services at a glance – jump straight to the topic you need.
The right design for every question
Contract Testing and Studies
From first hypothesis to conformity assessment – get the empirical foundation your development decisions rely on. Using state-of-the-art automated platforms for clinical chemistry and immunoassays, as well as methods such as ELISA and RT‑PCR, we identify the right measurement design for your study.
Exploratory Studies
Validate new development directions before committing resources. We test your hypotheses and new approaches – for example with human and animal serum samples – giving you a solid foundation for your next development step.
Feasibility Studies (Proof of Concept)
Identify risks before they become costly. A feasibility study under defined conditions gives you clarity on technical viability – so you can invest in larger studies with confidence.
Analyses from Small Sample Volumes
Get more from every sample. Even minimal volumes yield multiple parameters – conserving your valuable material while maximising the information content per sample.
Analytical and Clinical Performance Studies
Build the evidence base your submission needs. We evaluate the performance of your product (e.g. precision, sensitivity, specificity) and deliver all data compiled and ready for your Performance Study Report.
Point-of-Care Testing
Prove your product works where it matters most. Testing under real-world conditions demonstrates suitability directly in the target setting – giving you robust evidence for your intended use claim.
Multicentre Studies
Demonstrate reproducibility across sites – a key requirement for regulatory submissions. As your central laboratory or study partner, we ensure consistent, comparable results wherever your study runs.
Materials and processes that make your data reliable
Sample Preparation and Control Materials
The quality of your measurement results depends on the quality of the samples. We prepare your materials to accurately reflect your real-world conditions – for valid, reproducible data, even with small sample volumes.
Sample Preparation & Panel Assembly
- Assembly of customised sample panels for reproducible and comparable measurement runs
- Precise dilution, mixing, and enrichment of biomarkers, proteins, or other analytes
- Preparation of exact concentrations across different matrices to meet your study requirements
- Aliquoting for parallel analyses or long-term storage to optimise material use
- Handling of minimal volumes down to the microlitre range to preserve rare or valuable samples
- Ensuring homogeneity and quality of panels for reduced variability and greater reliability of results
Production of Reference & Control Samples
- Production of tailored reference and control materials
- Support for calibration, quality control, and proficiency testing
- Ensuring reliable results and consistent comparability across your measurements
Microbiology & Cell Culture
- Cultivation and propagation of cell lines and bacterial strains under controlled conditions
- Cell counting to ensure defined cell numbers
- Provision of cell-based assays
- Production of cell culture-based reference samples for realistic and reproducible testing conditions
Precision at the Microlitre Scale
Did you know? Thanks to our expertise and state-of-the-art technologies, we perform reliable analyses using sample volumes in the microlitre range. This conserves your valuable material and enables us to perform measurements that may not be possible elsewhere.
The Right Method for Every Requirement
From comparing different test systems to optimising existing methods, we combine a broad range of technologies with analytical precision and ensure that your assay performs optimally on the target system.
Strategic Consulting and Operational Support for Your IVD Studies
Good data is the beginning – but regulatory confidence, sound analyses, and compelling reports determine the success of your study. We support you from the initial idea through to study completion.
- Study and measurement design, Proof of Concept: We sharpen your research questions, develop appropriate study designs, and ensure efficient use of resources.
- Biostatistics consulting: We support you in statistical planning and evaluation – scientifically sound, robust, and audit-ready for regulatory requirements.
- Documentation and data transfer: We ensure complete, traceable documentation and structured data provision – audit- and submission-ready.
- Final report: We deliver a clearly structured, scientifically precise, and regulatory-ready summary of your study findings.
Complex studies and limited sample volumes require a partner who understands your needs – not one that simply generates measurement data points. With our scientific expertise and flexibility, we contribute to the success of your project. That is our commitment – driven by our standards and passion for keeping your studies in good hands.
– David Brodbeck, Head of Contract Laboratory
Get in Touch
Would you like to discuss a specific project, ask a question, or find out more about our services? Give us a brief outline of what it’s about – we will get back to you within 48 hours.
Email Address
Phone Number
Address
TRIGA-S GmbH
Mühltal 5, 82392 Habach, Germany
Send Us a Message
You Might Also Be Interested In
Clinical Study Supply Management
Sample Management
Services
Abbreviations
ELISA: Enzyme-Linked Immunosorbent Assay
ISO 13485: International standard for quality management systems (QMS) in the medical device industry
IVD: In vitro diagnostics
RT-PCR: Real-time quantitative polymerase chain reaction
BSL-2 Laboratory: Contract laboratory operating at Biosafety Level 2 (BSL-2)
