Author: seautaazad.bharti

Pharmaceutical Aerosols application, impacts of propellants on the environment and MCQs for GPAT, NIPER, Pharmacist and Drug Inspector exam

Pharmaceutical Aerosols Applications: They are used for their local action in the nasal areas, throat, and lungs, as well as for prompt systemic effect when absorbed from the lungs into the bloodstream (inhalation therapy). They are intended for topical application […]

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Pharmaceutical Aerosols: Components and MCQs for GPAT, NIPER, Pharmacist and Drug Inspector exam

Components of aerosols: Propellant Container Valve and actuator Product concentrate 1.Propellant – Responsible for developing proper pressure within the container.  Provide driving force to expel the product from the container. For detailed description on propellants refer to the article ‘Pharmaceutical […]

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Pharmaceutical Aerosols: Manufacturing and packaging methods and MCQs for GPAT, NIPER, Pharmacist and Drug Inspector exam

Packaging methods: Two methods have been used to package aerosol products. Unlike non-aerosol products, part of the manufacturing of necessity takes place during the filling operation. The propellant and product concentrate must be brought together in a way that ensures […]

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Pharmaceutical Aerosols: Propellants and MCQs for GPAT, NIPER, Pharmacist and Drug Inspector exam

Pharmaceutical Aerosols The propellant generally is regarded as the heart of the aerosol package. In addition to supplying the necessary force to expel the product, the propellant must also act as a solvent and diluent and has much to do […]

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Parenterals Product: IP injections, Sterile powders, Implants, Emulsions, suspensions and MCQs for GPAT, NIPER, Pharmacist and Drug Inspector exam

Sterile powders: Dry sterile powder is aseptically added to a sterile vial. The dry drug powder is reconstituted with a sterile vehicle before use. Powders for injections are solid substances, distributed in their final containers and which, when shaken with […]

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Parenterals product requiring sterile packaging: Production facilities and MCQs for GPAT, NIPER, Pharmacist and Drug Inspector exam

The production facility and its associated equipment must be designed, constructed, and operated properly for the manufacture of a sterile product to be achieved at the quality level required for safety and effectiveness. The processes used must meet cGMP standards. […]

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Parenterals product requiring sterile packaging: Production procedure (Part – II) Containers and Closures and MCQs for GPAT, NIPER, Pharmacist and Drug Inspector exam

Containers and Closures: Injectable formulations are packaged into containers made of glass or plastic. Container systems include ampoules, vials, syringes, cartridges, bottles, and bags. Ampoules are all glass, whereas bags are all plastic. The other containers can be composed of […]

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