Automating QC of Therapeutic Oligonucleotides in a Regulated Manufacturing Environment
Customer Company Size
Large Corporate
Region
- Europe
Country
- Germany
Product
- Genedata Expressionist
Tech Stack
- LC-UV-MS
- System Suitability Test
Implementation Scale
- Enterprise-wide Deployment
Impact Metrics
- Productivity Improvements
- Innovation Output
Technology Category
- Analytics & Modeling - Data-as-a-Service
Applicable Industries
- Pharmaceuticals
Applicable Functions
- Quality Assurance
Use Cases
- Predictive Quality Analytics
- Regulatory Compliance Monitoring
Services
- Data Science Services
- System Integration
About The Customer
Bayer Pharmaceuticals is a company that focuses on researching, developing, manufacturing and supplying specialty-focused innovative medicines that provide significant clinical benefit and value. The company obtained an exclusive license from Ionis Pharmaceuticals to develop new oligonucleotide-based treatments for a wide range of medical conditions. To support release testing and the imminent clinical trials of an advanced drug candidate, the Bayer Analytical Development Team for Biologics was tasked with implementing a validated drug substance and drug product release ID test. This required establishing new analytical methods, standard operating procedures, and organizational responsibilities.
The Challenge
Bayer Pharmaceuticals obtained an exclusive license from Ionis Pharmaceuticals to develop new oligonucleotide-based treatments for a wide range of medical conditions. To support release testing and the imminent clinical trials of an advanced drug candidate, the Bayer Analytical Development Team for Biologics was tasked with implementing a validated drug substance and drug product release ID test that required establishing new analytical methods, standard operating procedures, and organizational responsibilities. The tight go-live timeline and anticipated costs of any delay led Bayer to work together with our long-term partner Genedata to develop a confirmatory identification (ID) workflow of oligonucleotide species by mass spectrometry so that an approved quality control (QC) could be implemented and validated by Bayer’s Quality Assurance (QA) team. The main challenges were implementing an oligonucleotide analytics workflow, satisfying GMP requirements, and meeting a wide range of new analytical demands.
The Solution
Genedata Expressionist enabled timely implementation of highly customized MS solutions and thus the Ionis SOP could be swiftly translated into an automated end-to-end data processing, analysis, and reporting workflow. Together with Genedata consultants, Bayer further optimized the workflow at every processing step to meet its analytical needs and ensured compliance in Bayer’s regulated downstream operations, while adhering to the SOP. The ID test was based on analytical measurements that used MS and UV data independently and in combination. As an open and vendor-agnostic platform, Genedata Expressionist integrates seamlessly into the entire analytical process and enables Bayer to directly import and process raw data from different instruments and combine these data streams in a single analytical measurement. The Genedata Expressionist workflow developed for this project automatically determined the first acceptance criterion (the oligonucleotide ID) by reporting the m/z value of the main peak.
Operational Impact
Quantitative Benefit
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