September 12, 2022
Cleaning Validation In Pharmaceutical Industry
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…
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September 12, 2022
Validation VS Calibration
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 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…
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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 the pharmaceutical industry was introduced by the FDA due to issues with parenteral products when it comes to sterility. It is perhaps one of the most significant and most widely used terms in the industry, and its straightforward importance is to provide assurance when it comes to product…
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July 18, 2022
Disintegration and Dissolution
Disintegration and Dissolution Disintegration and Dissolution Disintegration and dissolution are the two most commonly used 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 an in vitro test that is performed utilising a basket rack assembly to check the…
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July 17, 2022
Thickness Test For Tablets
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…
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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 a 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. 1. Discovery and Preclinical Development: Sugar-coating should be possible in…
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July 10, 2022
Phases Of Sugar Coating
Phase 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…
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June 19, 2022
Standard Operating Procedure for Perforated Coating Pan System / Automatic Tablet Coater
Standard Operating Procedure for Perforated Coating Pan System / Automatic Tablet Coater The purpose of this SOP is to establish a standard procedure for operating the coating pan system. This will be applicable for the tablet coater in the coating area of the production section. A standard operating procedure (SOP) is a document that provides…
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June 19, 2022
Dosage Forms
Dosage Forms Dosage Forms Unit doses, likewise called dosage forms, are pharmaceutical drug products in the form in which they are advertised for use. Dosage forms are composed of a specific mixture of both active and inactive ingredients in a capsule shell (for example) and apportioned into a specific dose. For instance, two items may…
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