Expert Analytical Development
Veliter’s analytical development is the premier choice for analytical services covering all stages of drug development. Our 10’s years of analytical experience with oligonucleotides, together with our practical instrumentation, ensure reliable results to facilitate your program’s success.
Comprehensive solution from development to CMC/regulatory fillings
Veliter quality unit stays closely and stage by stage with you at every step of the drug development process—from method development, transfer, and validation to ICH stability studies to support CMC documentation for regulatory filings. The specialized challenges of oligonucleotide analysis, including raw materials, intermediates, adjuvants, APIs/DSs and DPs.
Phase-appropriate analytical development
Veliter quality unit stays closely and stage by stage with you at every step of the drug development process—from method development, transfer, and validation to ICH stability studies to support CMC documentation for regulatory filings. The specialized challenges of oligonucleotide analysis, including raw materials, intermediates, adjuvants, APIs/DSs and DPs.
Oligonucleotide sequencing
Liquid chromatography and electrospray ionization mass spectrometry (LC-ESI-MS/MS) will be utilized to sequence oligonucleotides. While oligonucleotides up to 50 bases are typically confirmed with 85%-100% coverage using the standard approach, oligonucleotides over 50 bases are subjected to specific enzyme digestions followed by LC-ESI-MS/MS. Veliter has experience on sequencing highly modified oligonucleotides within 150 nts.
Oligonucleotide quality control
To ensure the integrity of our facility and your oligo products, our Quality Control team performs test under the ICH requirements as follow:
- environmental monitoring;
- raw material, in-process and final product analysis;
- stability testing;
Most API and intermediate release testing is performed onsite, and offsite testing facilities (contract labs) are audited and approved periodically under our quality management system.
Our typical release testing include:
Appearance
pH
Molecular Weight
Sodium content (%w/w on anhydrous basis)
Molecular sequence
Residual solvents (head-space Capillary GC)
Identity by HPLC (IEX, SEC)
Halides
Thermal Melt (Tm)
Heavy metals (or full metal scan)
Purity and Impurity Profile (HPLC, UPLC, LCMS)
Bacterial endotoxins
Assay
Bioburden
Water content (%w/w)
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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