Dissolution Test in Tablet Formulation The dissolution test is a critical quality control test conducted during tablet formulation to assess the rate at which a […]
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What is disintegration test in tablet formulation?
Disintegration Test in Tablet Formulation The disintegration test is a crucial quality control test conducted during tablet formulation to assess how quickly a tablet disintegrates […]
How is a tablet’s hardness determined?
Determination of Tablet Hardness Tablet hardness, also known as tablet crushing strength, is a critical quality attribute that determines the tablet’s ability to withstand mechanical […]
What are the advantages of dry granulation over wet granulation?
Advantages of Dry Granulation Over Wet Granulation Advantages Dry Granulation Wet Granulation Drug Stability Dry granulation is suitable for moisture-sensitive drugs as it avoids exposure […]
Explain the process of dry granulation in tablet manufacturing
Dry Granulation in Tablet Manufacturing Dry granulation, also known as pre-compression or slugging, is a tablet manufacturing process that involves compacting the powder blend without […]
Explain the process of wet granulation in tablet manufacturing
Wet Granulation in Tablet Manufacturing Wet granulation is a widely used process in tablet manufacturing that involves the agglomeration of powder particles to form granules. […]
What are immediate-release tablets?
Immediate-Release Tablets Immediate-release tablets are a common type of pharmaceutical dosage form designed to release the active drug ingredient quickly after ingestion. These tablets are […]
Explain the role of GMP in preventing contamination and cross-contamination.
‘GMP helps in Preventing Contamination and Cross-Contamination’ Good Manufacturing Practice (GMP) plays a crucial role in preventing contamination and cross-contamination in pharmaceutical manufacturing. Contamination refers […]
How do GMP guidelines ensure product quality and safety?
‘GMP Guidelines Ensures Product Quality and Safety ‘ Good Manufacturing Practice (GMP) guidelines play a critical role in ensuring the quality and safety of pharmaceutical […]
What are the key principles of GMP?
Key Principles of Good Manufacturing Practice (GMP) in Pharmaceutical Manufacturing In pharmaceutical manufacturing, adhering to Good Manufacturing Practice (GMP) is crucial to ensure the quality, […]
What are the requirements for premises and equipment under Schedule M?
Premises and Equipment Requirements in Pharmaceutical Manufacturing Let’s explore the specific requirements for premises and equipment under Schedule M: 1. Premises Requirements Under Schedule M, […]
How is compliance with Schedule M ensured during drug manufacturing?
Ensuring Compliance with Schedule M during Drug Manufacturing Schedule M lays down stringent guidelines and requirements to ensure the quality, safety, and efficacy of drugs […]