Achieve your analytical objectives from process development to scale-up and cGMP manufacturing. When you partner with TriLink for oligonucleotide synthesis, custom chemistry, discovery mRNA synthesis services, or mRNA manufacturing, your project is accelerated by our in-house Analytical Services team with extensive expertise in nucleic acid characterization and analysis.
Analytical development and Quality Control expertise to support your project
The Analytical Development team evaluates your nucleic acid for the feasibility of generic methods and provides analytical method development and optimization for the characterization and analysis of nucleic acids.
Qualification and Validation
The Qualification and Validation team refines and develops methods to ensure robustness and reproducibility with a streamlined tech transfer of qualified and validated methods to our in-house QC team for on-site release testing.
The Quality Control team provides comprehensive testing for critical quality attributes, stability testing, and in-process and release testing.
Facilities and instrumentation
In 2022, TriLink expanded its in-house Analytical Services and Quality Control facilities, which house extensive state-of-the-art analytical instrumentation. Capabilities supported include stability studies, method development, qualification, and validation.
Culture of Quality
Our Analytical Services are critical to ensuring TriLink achieves manufacturing quality metrics that meet or exceed customer and regulatory expectations. Our ISO 9001 Quality Management System and team of quality experts ensure the highest level of consistency, purity, and comprehensive documentation.
Let’s discuss your needs!
Contact our team of experts to discuss your nucleic acid manufacturing, analytical development, and QC needs.