December 3, 2022
What is the Pharmaceutical Quality System?
What is the Pharmaceutical Quality System? The Pharmaceutical Quality System (PQS) is a set of guidelines that pharmaceutical companies must adhere to in order to ensure the quality and safety of their products. The PQS covers all aspects of the drug manufacturing process, from research and development to production and distribution. It is essential for ensuring…
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November 19, 2022
Quality Auditing in Pharmaceutical Industry
Quality Auditing in Pharmaceutical Industry Quality auditing is an integral part of the pharmaceutical industry. It ensures that products meet all government regulations and standards for safety and efficacy, as well as customer requirements. Quality auditing helps to ensure product quality by examining processes, materials, methods, systems, and services used at each stage of drug development…
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September 12, 2022
Cleaning Validation In Pharmaceutical Industry
Cleaning Validation In Pharmaceutical Industry In the pharmaceutical industry, cleaning validation is the process of substantiating the cleaning strategy during manufacturing. Cleaning Validation is the system used to guarantee that a cleaning cycle eliminates buildups of the dynamic drug elements of the item made in a piece of hardware, the cleaning helps used in the…
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September 12, 2022
Validation VS Calibration
Validation VS Calibration The FDA first established the idea of validation in 1979 in an effort to raise product quality. Validation is documented evidence that provides the confidence that a process will consistently result in a product with the pre-specified requirements and quality. It is a process, procedure, or action that must be validated in writing…
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August 7, 2022
Good Manufacturing Practice (GMP)
Good Manufacturing Practice (GMP) Good Manufacturing Practice (GMP) is a set of guidelines introduced by the US Food and Drug Administration (FDA). It is a framework for guaranteeing that products are reliably created and controlled by quality principles. It is intended to limit the dangers implied in any pharmaceutical production that can’t be dispensed with…
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July 28, 2022
Pharmaceutical Validation
Pharmaceutical Validation The idea of Validation in pharmaceutical industries was introduced by the FDA due to the issues of parenteral items when it comes to sterility. It is perhaps one of the most significant and most used terms in the industry, and its straightforward importance is to provide assurance when it comes to product quality…
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July 18, 2022
Disintegration and Dissolution
Disintegration and Dissolution Disintegration and dissolution are the two most commonly involved terms in the pharmaceutical industry. However, a large portion of individuals don’t have a clue about the specific contrast between these two terms. Disintegration is the vitro test that is performed utilising a basket rack assembly to check the rate at which the…
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July 17, 2022
Thickness Test For Tablets
Thickness Test For Tablets The test utilised to quantify how thick the tablet is is known as the tablet thickness test. To guarantee that the thickness of each tablet is within the predefined range as referenced in BMR, a thickness test for tablets is initially conducted after line clearance. Afterwards, it is worth taking a…
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July 11, 2022
The Process of Sugar-Coating
The Process of Sugar-Coating The process of sugar-coating includes the progressive deposition of watery sugar solution on the tablet cores as they are rotated and tumbled in a rotating dish by splashing sugar solutions or suspensions into a skillet and drying off the solvent. Benefits Of Sugar Coating Sugar-coating should be possible in a regular…
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July 10, 2022
Phases Of Sugar Coating
Phase Of Sugar Coating In 1953, Abbot Laboratories launched the first sugar-coated tablet. It was first created by the French in mid of 1800. The first patent was issued in 1837. Then, it was initially applied to the pills of Cubeb and Copaiba in 1840. The strategy of sugar-coating was then spread to the United…
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