by Naveen kumar | Nov 28, 2024
Out of Specifications (OOS) in Pharmaceuticals Out of Specification (OOS) results occur when the test results of a pharmaceutical product fall outside the predefined acceptance criteria specified in regulatory guidelines or quality standards. These deviations are...
by Naveen kumar | Nov 13, 2024
In the world of pharmaceuticals, Active Pharmaceutical Ingredients (APIs) and Intermediates are essential yet distinct parts of the drug manufacturing process. Understanding Active Pharmaceutical Ingredients (APIs) An API is the core component of a drug, directly...
by Naveen kumar | Oct 27, 2024
Ensuring Quality in Tablet Manufacturing: The Essential Role of Critical Quality Attributes (CQAs) Introduction In the pharmaceutical industry, ensuring the consistent quality, safety, and effectiveness of products is non-negotiable. Tablets, one of the most common...
by Naveen kumar | Oct 13, 2024
Compression, Compaction, and Consolidation: The Pillars of Tablet Manufacturing In the world of pharmaceutical manufacturing, producing a high-quality tablet is no simple task. Behind every solid, consistent tablet lies a carefully controlled process involving...
by Naveen kumar | Oct 13, 2024
The Role of Precompression Rollers in Tablet Compression In pharmaceutical manufacturing, the tablet compression process is a critical step in ensuring the quality of the final product. One essential component that plays a significant role in this process is the...
