Tag: General Article
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Manufacturing Defects of Tablets
Manufacturing Defects of Tablets processing problems can be due to the problem in the formulation or in the compression equipment, or both of them. Thus…
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Overview of 21CRF
21CFR is the code of federal Regulation. It is the regulation which gives by the USA/America for the pharma Industries. 21CRF It is started in…
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Biowaivers
Biowaivers are a means of waiving bioequivalence studies in humans. Although, in theory, simultaneous dossier submissions can greatly streamline the drug approval process, in practice,…
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Tablet Scoring in Pharmaceuticals
Tablet Scoring in Pharmaceuticals An emerging concept in the pharma industry, Tablet Scoring in Pharmaceuticals refers to the breakage of a tablet to attain a…
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Tablet Scoring: Challenges and Opportunities
Tablet Scoring: Challenges and opportunities are describe in this post. Tablet splitting can lead to medication errors. One of the main reasons is that the…
