By treating distinct validation guidelines as decision-making units, data envelopment analysis (DEA) allows for the mathematical evaluation of their resource efficiency.
- You Can't CAPA What You Can't Classify
- 6 Modeling Approaches That Make Complex Bioprocess Data Useful
- Building Trust In AI For Computerized System Validation
- A Gentler Cell Line Selection Method Using microRNA
- Controls For Retrieval-Augmented Generation In GxP
- Implementing AI Solutions In GMP While Managing Risk
- Implementing And Optimizing Your eQMS
GUEST COLUMNISTS
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You Can't CAPA What You Can't Classify
An LLM or agentic error can occur with no component broken in any way the QMS recognizes. Classifying it takes two fields: the error type and the error origination point.
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6 Modeling Approaches That Make Complex Bioprocess Data Useful
AI algorithms can reduce data dimensionality more faithfully by interpreting multivariate features relevant to prediction or control.
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Building Trust In AI For Computerized System Validation
Using AI for CSV might feel like the students are grading their own papers. One consultant explains why it's not the same, namely, there are no subjective judgment calls.
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A Gentler Cell Line Selection Method Using microRNA
Traditional selection stresses surviving cells. New research shows how structurally interacting RNA may use endogenous microRNA for a faster, nontoxic selection process.
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Controls For Retrieval-Augmented Generation In GxP
Validation teams deal with inherent variability all the time. The same principles for GMP — think visual inspection — can apply to probabilistic AI systems.
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Implementing AI Solutions In GMP While Managing Risk
When using artificial intelligence in GMP settings, risk management extends far beyond validation. This discussion explores moving AI solutions out of the pilot phase.
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Implementing And Optimizing Your eQMS
This article addresses everything that follows the signed contract for an eQMS: how a system is configured, validated, adopted, and maintained.
BIOSIMILAR WHITE PAPERS
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Economic Advantage Of Robotic Gloveless Pharmaceutical Isolators
Are robotic gloveless isolators the key to smarter, safer, scalable solutions? Discover how they can revolutionize aseptic filling by reducing contamination, minimizing waste, and enhancing manufacturing flexibility.
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Optimizing Safety Measures For rAAV Therapies10/11/2024
Explore common process-related impurities found in recombinant Adeno-Associated Virus (rAAV) vectors and the analytical testing methods used for these residuals.
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A Comprehensive Solution For Adventitious Agent Testing2/13/2026
Modern sequencing methods offer sensitive detection of adventitious and species‑specific viruses. Learn how targeted and non‑targeted NGS approaches improve confidence in cell bank characterization.
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Why Choose Robotic Processing For Small Batch Aseptic Filling1/9/2026
Reducing human intervention in aseptic filling is critical for safety and cost efficiency. Learn why automation is essential for small-batch applications and how it’s transforming sterile drug manufacturing.
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Assessing A Targeted Molecular Method Against Traditional In Vitro Testing For Adventitious Virus Detection10/3/2024
Discover a CHO AOF panel that provides rapid detection of relevant adventitious viral contaminants in bulk harvest material, and explore data showing equivalent sensitivity to the in vitro assay.
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How Lipid Nanoparticles Enable Next-Gen Delivery10/20/2025
Cell therapy’s future depends on smarter gene delivery. Learn how lipid nanoparticles offer a scalable, cell-friendly alternative to electroporation and viral vectors for manufacturing efficiency.
BIOSIMILAR APP NOTES & CASE STUDIES
- Cell Culture Media Filtration: Evaluating Cell Culture Performance
- Multi-Column Chromatography For Efficient Polishing Purification
- Optimizing TFF And SPTFF For High-Concentration mAb Formulations
- CDMO Uses Robotic Gloveless Isolator For Advanced Therapeutics
- Cell Culture Media Mixing In A Benchtop Single-Use Mixer
BIOSIMILAR DEVELOPMENT CONTENT COLLECTIONS
The debate over whether the biosimilar regulatory paradigm can shift away from comparative efficacy trials has intensified over the past few years. This collection of articles serves as a snapshot of the many different components of this ongoing discussion.
More Content CollectionsBIOSIMILAR DEVELOPMENT NEWS
- Waltz Health And Fresenius Kabi Expand Direct Access To Biosimilars Through Waltz Connect Platform
- The Biosimilars Forum Strongly Supports FDA's BsUFA IV Agreement To Strengthen Biosimilar Development And Review
- Sandoz Opens Advanced High-Volume Drug Substance Manufacturing Centre In Lendava, Significantly Strengthening In-House Capacity And Flexibility Across Leading European Biosimilar Network
- STADA And SBP Group Launch Strategic Biosimilars Partnership, Including A Biosimilar To Keytruda
- Meitheal Pharmaceuticals Announces FDA Approval Of High-Concentration Formulation Of YUSIMRY, A Biosimilar To Humira
- Teva Continues Biosimilar Momentum With U.S. FDA Approval Of DEGEVMA™ (denosumab-adet), A Biosimilar To Xgeva® (denosumab)
- AAM And Biosimilars Council Comment On GDUFA And BsUFA User Fee Negotiations And Reauthorization
- PhRMA Statement On The Biosimilar User Fee Act (BsUFA) IV Performance Goals Letter
NEWSLETTER ARCHIVE
- 10.01.26 -- Faster Paths To Biosimilar Equivalence
- 09.24.26 -- Navigating The Regulatory Space To Biosimilar Approval
- 09.17.26 -- Your Collaborator: mAb Productivity And Robustness
- 09.17.26 -- A Much-Improved Approach For Managing Safety Risks
- 09.16.26 -- Smarter Ways To Reduce Risk, Downtime, And Lifecycle Surprises