Move to the clinic with confidence
Anticipate and overcome manufacturing & regulatory challenges
When you have a promising drug candidate, choosing a supplier and mRNA manufacturer with the capacity and expertise to orchestrate these complex operations can be the key to successful clinical stage progression. TriLink® equips your clinical development project with extensive experience, technical expertise, and scalability to ensure quality and efficiency every step of the way.
Prepare earlier with GMP-grade materials
Focusing on GMP-grade raw materials and manufacturing early in your development journey can help you scale up the appropriate materials. TriLink has protocols in place to manufacture and scale up to GMP-grade materials as needed. Partnering with TriLink ensures access to phase-appropriate materials and manufacturing for your clinical development program.
GMP-grade CleanCap® technology
Our flagship capping technology is available in GMP-grade to meet any scale of production.
GMP-grade modified uridine nucleosides
The extensive TriLink® catalog of modified nucleoside triphosphates, available from RUO to GMP-grade, provides the highest quality NTPs for any application.
mRNA expertise to eliminate unknowns in your drug substance manufacturing
From discovery to final drug substance, partnering with TriLink ensures access to phase-appropriate materials and manufacturing for your clinical development program. By working with an experienced CDMO partner, you can anticipate and avoid potential challenges and hurdles in manufacturing scale-up and recover quickly from any unavoidable obstacles.
High-quality plasmid DNA
Phase-appropriate, high-quality plasmid DNA templates to support your mRNA therapeutic and vaccine programs.
Clinical mRNA synthesis
TriLink offers a wide selection of DNA, RNA, modified, and specialty oligonucleotides in scales up to multiple grams. We specialize in the synthesis of difficult and unusual constructs.
Analytical services
In-house capabilities powered by our Analytical Development and Quality Control teams with extensive expertise in nucleic acid characterization and analysis.