Zeneth
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- 20 tips for nitrosamine impurity assessment
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Related Publications
- 1. Qualifying impurities and degradation products: Anvisa's experience and technical improvement - Maria Rodrigues (Video)
- 2. Risk assessment of potential mutagenic impurities in anti-hypertensive drug products approved in Brazil - Fernanda Waechter (Slides)
- 2. Risk assessment of potential mutagenic impurities in anti-hypertensive drug products approved in Brazil - Fernanda Waechter (Video)
- 2019 Webinar Zeneth 8: A faster, more intuitive, degradation predictive system - Recording
- 2019 Webinar Zeneth 8: A faster, more intuitive, degradation predictive system - Slides
- 2020 Zeneth 8 webinar - Zeneth 8: A re-designed and improved forced degradation prediction system for organic compounds - Recording
- 2020 Zeneth 8 webinar - Zeneth 8: A re-designed and improved forced degradation prediction system for organic compounds - Slides
- 3. Case studies on the qualification of impurities - Mariah Ultramari (Slides)
- 3. Case studies on the qualification of impurities - Mariah Ultramari (Video)
- 46th ICGM Product Manager Update
- 49th ICGM Product Manager Update
- A Case Study in Predicting hERG Activity.
- A collaborative benchmarking study to evaluate the newly released Zeneth 8
- A knowledge-based system for the prediction of forced degradation of organic compounds
- A Suggested ICH M7 Framework Using Lhasa Limited Products
- An Expert System To Predict the Forced Degradation of Organic Molecules
- An Overview of Lhasa Limited Collaborative Data Sharing Initiatives
- Automated chromophore identification to support prediction of light-mediated reactivity
- Chapter 17: In Silico Drug Degradation Prediciton
- Chapter 17: Use of Lhasa Limited Products for the In Silico Prediction of Drug Toxicity
- Enhancing carbon acid pKa prediction by augmentation of sparse experimental datasets with accurate AIBL (QM) derived values
- How Zeneth fits into ICH Q3D
- ICH M7 Brochure
- ICH M7 Workshop - 2020 ICH M7 India Roadshows
- Impact from the Recent Issuance of ANVISA Resolution RDC-53/2015 on Pharmaceutical Small Molecule Forced Degradation Study Requirements
- In silico prediction of N-nitrosamine degradants in APIs that possess a secondary or tertiary amine functional group
- In Silico Prediction of Pharmaceutical Degradation Pathways: A Benchmarking Study
- In Silico Predictive Approaches to Degradation Using Zeneth
- Increased Efficiency in Knowledge Base Building for Degradation
- Mutagenic Impurities: Precompetitive/Competitive Collaborative and Data Sharing Initiatives
- Mutagenicity Prediction Using In Silico Methods: Gigabyte-Sized Petri Dishes
- Next Generation Zeneth: Software and Science Proposals
- Product Update 2019
- RDC53: Challenges on impurities qualification
- Save Time and Money with Lhasa Limited
- The application of in silico models to support decision making in toxicology
- Toxicity Evaluation of Degradation Products
- Use of In Silico for Assessing Degradants
- Zeneth 2018.1.0 Release Notes.pdf
- Zeneth 7 Installation Guide
- Zeneth 7 Z2016.1.1 Release Notes
- Zeneth Brochure
- Zeneth Member Type Infographic
- Zeneth Tutorial Adding Patterns
- Zeneth Tutorial Adding Transformations
- Zeneth Tutorial AutoZeneth
- Zeneth Tutorial Creating Reports
- Zeneth Tutorial Processing Against Excipients
- Zeneth Tutorial Processing Structures
- Zeneth Tutorial Reasoning in Zeneth
- Zeneth Tutorial Zeneth Results
- Zeneth: an in silico tool to aid identification of degradants