Nitrosamine Impurities in Pharmaceuticals: Critical Guide
Learn about nitrosamine impurities in pharmaceuticals, including causes, FDA limits, regulations, risk assessment and mitigation strategies.
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Learn about nitrosamine impurities in pharmaceuticals, including causes, FDA limits, regulations, risk assessment and mitigation strategies.
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Explore common types of nitrosamine impurities in pharmaceuticals, including NDMA, NDEA and NDSRIs. Learn about examples, FDA AI limits and risk assessment.
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How are nitrosamines formed in pharmaceuticals? Learn 5 critical causes, including nitrite, amines, excipients, formulation, manufacturing and storage risks.
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Learn what nitrosamines are, how they form in pharmaceutical products, common nitrosamine impurities, NDSRIs, risk factors and mitigation strategies.
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Why are pharmaceutical excipients important? Learn how excipients support drug stability, release, manufacturing, quality, and patient acceptability.
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Discover pharmaceutical excipients, their types, functions, applications, benefits and selection criteria, with practical examples for drug formulation.
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Compare 101 vs 102 to understand key differences and applications, and choose the right microcrystalline cellulose grade for tablet formulation.
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Discover how SANCEL™ Low Nitrite Microcrystalline Cellulose helps reduce nitrosamine risk while delivering reliable performance for pharmaceutical formulations.
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Learn what Microcrystalline Cellulose is, its benefits, uses, properties, and role in pharmaceutical formulations with this expert guide from NB Entrepreneurs.
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Discover STARCEL™ Silicified Microcrystalline Cellulose for improved flowability, compressibility, and direct compression in tablet manufacturing.
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Discover why Co-Processed Excipients are preferred for modern tablet manufacturing with better flowability, stability & compression performance.
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A complete buyer’s guide to choosing a pharmaceutical excipient manufacturer in India, certifications, MCC grades, red flags, key documents & 10 must-ask questions before ordering.
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Learn how to choose the right excipients for tablet formulation to improve tablet quality, manufacturing efficiency, and pharmaceutical performance with NB Entrepreneurs.
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In initial days of the tablet, manufacturing tablets were produced with manually operated machines, which suffered many problems. But even with the advent of modern electronic machines many problems of tablet manufacturing still persist. A modern tablet production unit a rule experiences number of issues during production. A perfect tablet ought to be free from […]
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Drug degradation is one of the issues that pharma company’s face and are searching for controlling it. Drug degradation results from the interaction of API and excipient. Excipients impurities are the components that are harmful to the stability of drug product. Understanding of excipient is must for designing and developing a medicine. This element should […]
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Learn the complete tablet processing workflow, including direct compression, wet granulation, and dry granulation with NB Entrepreneurs’ premium pharmaceutical excipients.
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Modified pharmaceutical excipients, including spray-dried, co-processed, physically modified and multifunctional excipients for pharmaceutical formulations.
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If we want to define quality, we will say that it is conforming to the earlier-defined specification or meeting expectations. However, quality is a relative term. For some, it may be excellence; for some, it is value for money or just convenience. It is a multifaceted concept, having different levels of dimensions, but it is […]
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Microcrystalline cellulose for direct compression, highlighting QbD, critical material attributes, binding, compressibility, and tablet quality.
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Excipients affect drug quality by influencing stability, dissolution, bioavailability, manufacturability, tablet performance, and overall product consistency. Their physical and chemical properties, purity, variability, and compatibility with the API can directly influence critical quality attributes of the finished pharmaceutical product. Nowadays, these quality, well-being, and viability of the items are the prime necessities. Subsequently, the regulatory […]
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Actively used in the pharmaceutical market, this super disintegrant is commonly used as an additive. The additive enjoys its position in the market where it has been approved by the U.S. Food and Drug Administration. Mainly used in tablets including dietary supplements, it has several amazing features that add to its already long list of […]
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Physical properties of a material and its behaviour in surroundings get affected by its porosity. How a substance can be used largely depends on its adsorption, permeability strength and density. Porosity is a property that impacts a significant number of the CQA of final pharmaceutical items. Porosity can help foresee distortion properties amid compression, pharmacokinetic […]
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Since the inception of NB Entrepreneurs, we paid sheer interest in meeting our customer and connecting with our fellow companions. This year, we are immensely delighted to inform you that we will be participating in CPhI Worldwide as an Exhibitor at Madrid, Spain during 9th-11th October 2018. As, NB Entrepreneurs stand tall with the mission […]
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Microcrystalline Cellulose (MCC) is one of the most widely used pharmaceutical excipients for tablet manufacturing. But MCC does not simply come from wood pulp and go directly into a tablet. Its transformation involves controlled processing that gives cellulose the physical and functional properties required for pharmaceutical applications. From cellulose purification and controlled hydrolysis to particle […]
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Magnesium Stearate is the most popular excipient used in pharmaceutical industry. It is a versatile component and can be used as a flow agent, lubricant etc. It is made up of two important components; magnesium and stearic acid. It is used not only in pharma industry but also in various industries like dietary supplements and […]
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