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    Pharmaceutical analysis

    Atomic Absorption Spectroscopy in drug testing and analysis

    To ensure the safety, quality and efficacy of compounds being produced, USP has developed standards and guidelines that must be observed by the pharmaceutical industry. Preferences of UV/Vis Spectroscopy Simple to utilize Straight forward structure of instrument utilizes the light from a specific light to go through the example Quick outcomes Rapidly investigates HPLC (High-performance

    Pharmaceutical Roots – Almonds and Enantiomers

    Pharmaceutical roots is a new series from LGC Mikromol, investigating and outlining the natural origins of pharmaceutical substances, and offering a deeper dive into their uses, risks, and mechanisms of action. Mandelic acid Mandelic acid is a small, aromatic compound with many different uses. Although these days it is usually prepared in the lab, mandelic

    Quality Control of Pharmaceuticals using Titration Techniques

    With regard to the quality and safety of drugs, authorities worldwide set high standards for the pharmaceutical industry. These are documented in pharmacopoeias in the form of official collections of recognized pharmaceutical rules. As legal tools of consumer protection, they ensure that drugs are used safely. It is only the measuring and test procedures used

    Fast & Accurate Moisture Content Determination in Pharmaceuticals with Halogen Moisture Analyzer HX204

    Moisture content determination is an important quality control test in pharmaceutical manufacturing, from the checking of incoming raw materials and in-process control of tablets and capsules to undertaking quality checks of finished drugs as part of pharmacopeial testing procedures. Moisture testing is also one of the critical quality parameters in the stability testing of drugs.

    LGC: a leading global manufacturer and provider of reference standards

    Microbioz India is pleased to share an exclusive interview with Suryakanth Gudgunti, LGC’s Business Development Manager for India, the Middle East and Southwest Asia. Based in Mumbai, India, Suryakanth works in LGC’s pharmaceutical go-to-market team, and is a government registered pharmacist with 24 years of experience in the field of reference standards and impurities. He

    Pharmaceutical Analysis: What effect does particle size have on solubility?

    In the pharmaceutical industry, particle size is a key factor since it affects surface area and porosity, which in turn affects a drug’s bioavailability, effectiveness, and shelf life. Particle size is therefore examined in the creation of new active medicinal components as well as in quality control (APIs). In fact, while assessing novel medications, particle

    The Science of Drug Analysis: All you need to know

    The identification of new medications, measurement of binding affinity and selectivity, characterization of molecular structures, and evaluation of efficacy through in vitro and in vivo studies are all components of drug testing and analysis. Nuclear magnetic resonance (NMR) spectroscopy is commonly utilized in the screening of new pharmacological compounds, as well as structural analysis and

    Metals Analysis in Pharmaceutical Goods

    Pharmaceutical element analysis and trace metals analysis are crucial for drug product quality management and commercial release. Understanding the elemental composition of your raw materials, active pharmaceutical ingredients (APIs), excipients, or formulations aids in the quality and purity of your product. When the elemental composition is unknown, a strategic strategy is essential to rationalize effort