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Tag: Manufacturing guidelines

What are the different methods of tablet coating?

Posted on August 17, 2023August 5, 2023 By Admin

Different Methods of Tablet Coating Tablet coating is a process used to apply a thin layer of coating material onto the surface of tablets. The coating can serve various purposes, including improving tablet appearance, taste masking, providing gastro-resistance, or modifying drug release characteristics. There are different methods of tablet coating, each with its own advantages…

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Tablets

How is tablet stability determined and tested?

Posted on August 17, 2023July 31, 2023 By Admin

Tablet Stability Testing Tablet stability testing is a critical aspect of pharmaceutical development and quality control. It involves evaluating the chemical, physical, and microbiological properties of tablets over time to ensure their quality, safety, and effectiveness throughout their shelf life. The stability testing process follows established guidelines and regulatory requirements to assess how the tablets…

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Tablets

Explain the role of lubricants in tablet compression.

Posted on August 16, 2023August 5, 2023 By Admin

Role of Lubricants in Tablet Compression Lubricants play a crucial role in tablet compression, as they are essential for ensuring the smooth and efficient operation of the tablet manufacturing process. Lubricants are inactive ingredients added to the tablet formulation to reduce friction between the tablet blend and the surfaces of the tablet press during compression….

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Tablets

How are tablet defects identified and rectified?

Posted on August 15, 2023August 5, 2023 By Admin

Identification and Rectification of Tablet Defects Tablet defects can arise during tablet manufacturing due to various factors, including formulation issues, process challenges, equipment problems, and environmental conditions. Identifying and rectifying tablet defects are crucial to ensure the production of high-quality tablets that meet the required specifications and regulatory standards. Here are the steps involved in…

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Tablets

What are the key elements of a tablet formulation development process?

Posted on August 15, 2023July 31, 2023 By Admin

Key Elements of Tablet Formulation Development Process The tablet formulation development process is a critical stage in the pharmaceutical product development life cycle. It involves designing a tablet formulation that ensures the stability, bioavailability, safety, and effectiveness of the drug product. The process requires careful consideration of various factors and the integration of scientific principles…

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Tablets

What are the critical factors affecting tablet uniformity during production?

Posted on August 14, 2023August 5, 2023 By Admin

Critical Factors Affecting Tablet Uniformity during Production Achieving tablet uniformity during production is essential to ensure that each tablet in a batch contains the correct amount of active pharmaceutical ingredient (API) and other excipients. Tablet uniformity directly impacts the drug’s efficacy, safety, and patient compliance. Several critical factors can influence tablet uniformity during production, and…

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Tablets

How is tablet dissolution testing performed?

Posted on August 14, 2023July 31, 2023 By Admin

Tablet Dissolution Testing Tablet dissolution testing is a critical quality control test used to assess the rate at which a tablet disintegrates and releases its active pharmaceutical ingredient (API) in a specified dissolution medium. It provides valuable information about the tablet’s drug release profile, which is essential for ensuring the tablet’s bioavailability and effectiveness. Here’s…

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Tablets

How are enteric-coated tablets prepared?

Posted on August 13, 2023August 5, 2023 By Admin

Preparation of Enteric-Coated Tablets Introduction to Enteric-Coated Tablets Enteric-coated tablets are designed to bypass the acidic environment of the stomach and release the medication in the alkaline environment of the small intestine. This coating is essential for drugs that are sensitive to stomach acid or cause gastric irritation. The enteric coating allows for delayed or…

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Tablets

How are medical devices labeled and tracked for traceability?

Posted on August 13, 2023August 2, 2023 By Admin

Labeling and Traceability of Medical Devices Labeling and traceability are essential aspects of medical device manufacturing and distribution, ensuring that devices can be identified, tracked, and traced throughout their entire lifecycle. Proper labeling and traceability systems provide valuable information for regulatory compliance, quality control, post-market surveillance, and patient safety. Here’s how medical devices are labeled…

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Medical Devices

Explain the concept of tablet weight uniformity and its acceptance criteria.

Posted on August 13, 2023July 31, 2023 By Admin

Tablet Weight Uniformity and Acceptance Criteria Tablet weight uniformity is a critical quality control parameter in tablet manufacturing. It refers to the consistency of the weight of individual tablets within a batch. Ensuring tablet weight uniformity is essential because variations in tablet weight can lead to differences in drug content, which can affect the drug’s…

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Tablets

Explain the process of direct compression for tablet manufacturing.

Posted on August 12, 2023August 5, 2023 By Admin

Process of Direct Compression for Tablet Manufacturing Introduction to Direct Compression Direct compression is a widely used method for tablet manufacturing in the pharmaceutical industry. It involves the direct compression of a blend of active pharmaceutical ingredients (APIs) and excipients into a tablet without the need for granulation or additional processing steps. This process is…

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Tablets

What are the potential issues with medical device surface finish and coatings?

Posted on August 12, 2023August 2, 2023 By Admin

Potential Issues with Medical Device Surface Finish and Coatings The surface finish and coatings of medical devices play a crucial role in their performance, biocompatibility, and safety. However, various potential issues may arise with these aspects, impacting the device’s functionality and patient outcomes. Here are some common issues associated with medical device surface finish and…

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Medical Devices

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  • Aerosol Formulations
  • Capsules (Hard & Soft Gelatin)
  • Drug Discovery
  • External Preparations
  • GLP Guidelines
  • GMP Guidelines
  • Medical Devices
  • Parenteral Drug Manufacturing
  • Pharma Quality Control
  • Pharma Research
  • Schedule M
  • Solid Dosage form
  • Solid Oral Dosage Forms
  • Tablets
  • Tablets

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