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Parenteral Solutions in Argentina: What Changes Under ANMAT Regulation 5146/2026?
ANMAT Regulation 5146/2026 clarifies the requirements for closed manufacturing systems used in large-volume parenteral solutions. Learn how these requirements relate to pharmaceutical quality control and subvisible particle testing.
Subvisible Particles in Injectables: Analytical Criteria and Compliance with the Argentine Pharmacopoeia
Technical review of Argentine Pharmacopoeia requirements for subvisible particles in injectables, covering sample preparation, acceptance criteria, analytical limitations and HIAC 9703+ applications.
ANMAT: What Is Required in a Good Manufacturing Practices Inspection
ANMAT Disposition 4159/23 defines GMP requirements for pharmaceutical manufacturers in Argentina, covering quality systems, facilities, equipment, documentation, qualification, validation and quality control.
Why do some surfactants better protect therapeutic proteins against agitation-induced aggregation?
Protein and surfactant compete for the same air/water interface, and whichever arrives first determines the fate of the batch. Adsorption kinetics, not CMC, correlates with agitation-induced aggregation.
MISEV: Complete Guide to Extracellular Vesicle Studies
A practical guide to MISEV2023 recommendations for rigorous and reproducible extracellular vesicle studies, covering nomenclature, pre-analytical variables, separation, characterization, functional assays and transparent reporting.
Analysis of Lipid Nanoparticles (LNPs) for mRNA Delivery with ZetaView®
Las nanopartículas lipídicas para la entrega de ARNm: ZetaView mide tamaño, concentración, potencial zeta mediante NTA/fluorescencia, garantizando estabilidad y calidad.
MOF for CO₂ Capture: Co-adsorption in Humid Conditions - A Case Study
Study reveals how a novoMOF MOF maintains high efficiency in CO₂ capture under humid conditions using the DVS Carbon and BTA Frontier instruments.
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