Expert Process Development
Based on our best-view platform, Veliter’s Process Development offers industry-leading development services to solutions tailored to individual customer needs, from the lab to validation and commercial manufacture. Our experts team will ensure our approaches are aligned with regulatory guidelines and GMP industry best practices.
Experience makes the difference
Veliter’s development and scale-up experience covers various therapeutic oligonucleotide modifications (special nucleotides, PS/PN replacement of PO, chemical modification on 2’ position of nucleotides, 2’-4’ locked nucleotides, chemical modification on phosphorus, conjugated oligonucleotides,etc) in the market. Our technical team constantly explores and brings you emerging chemical modifications and processes.
Process or transfer
A customized oligo process can come from your development team after technical transfer or directly from Veliter’s process development. Through our VPS™ program, Veliter can offer a starting point for development to reduce development time and minimize manufacturing risk at the same time.
Customized approach
Your project is unique in entire development. Veliter provides solutions tailored for your project including: facility risk assessments, small scale modeling of large scale manufacturing, product specification development/justification, raw material vendor selection and qualification, and a dedicated manufacturing project manager.
Commercial offer
Veliter is capable of supporting you with commercial oligonucleotides and beyond.
Process development capabilities:
- Synthesis, cleavage and de-protection, purification, and downstream processing of various complex and modified DNA, RNA and analogue oligonucleotides
- Pre-clinical non-GMP and GMP-like oligo production
- Process parameter screening and robustness testing using Design of Experiments
- PS, PO, PN and mixed backbone sequences
- Conjugation including GalNAc,PEG and analogues etc.
- Sequences from <10 to <150 bases
- Process Performance Qualification activities and support
Positive oligo program experience, from end to end
Focusing on your needs and building long-term partnerships, your own Veliter’s project manager will be flexible and responsive. This is Veliter’s approach to make your oligonucleotide program move smoothly through pre-clinical to commercial.
Products & Services
Preclinical Manufacturing
Veliter’s VPS™ (Veliter Preclinical Service)provides affordable, quality oligonucleotides with fast turnaround times...
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Expert Analytical Development
Veliter’s analytical development is the premier choice for analytical services covering all stages of drug development...
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Expert Process Development
Based on our best-view platform, Veliter’s Process Development offers industry-leading development services to solutions...
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Drug Substance (API) Manufacturing
Premier partner from preclinical to commercial supply – Veliter is one of few real Oligonucleotide CDMO across the world currently...
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Drug Product Formulation & Manufacturing
Veliter is an expert partner handling the entire process—from API (drug substance) development through fill finish manufacturing of drug product...
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Validation / Process Performance Qualification
Ensure clearing to commercial manufacturing – Based on the requirement of consistency and reproducibility in pharmaceutical manufacture...
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Quality Control & Stability Study
Understanding the vital role that quality control testing and stability study play in all facets of your project, Veliter’s QC group has the expertise and resources for you to keep your project on track.
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