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Tag: Pharmaceutical manufacturing

What are the common problems encountered in tablet manufacturing?

Posted on August 11, 2023August 5, 2023 By Admin

Common Problems Encountered in Tablet Manufacturing Tablet manufacturing is a complex process that involves several steps and numerous factors that can influence the final product’s quality. Despite careful planning and control, various challenges may arise during tablet production. Some of the common problems encountered in tablet manufacturing include: 1. Content Uniformity Issues Inadequate mixing of…

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Tablets

What are the challenges in manufacturing capsules with highly potent APIs?

Posted on August 11, 2023July 31, 2023 By Admin

Challenges in Manufacturing Capsules with Highly Potent APIs Manufacturing capsules with highly potent active pharmaceutical ingredients (APIs) presents unique challenges due to the increased risk associated with handling and processing these potent compounds. Highly potent APIs are those that have a pharmacological activity at very low doses, often in the microgram or even nanogram range….

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Capsules (Hard & Soft Gelatin)

What are the key factors influencing the bioavailability of tablets?

Posted on August 11, 2023July 31, 2023 By Admin

Key Factors Influencing the Bioavailability of Tablets Bioavailability refers to the extent and rate at which the active pharmaceutical ingredient (API) in a tablet is absorbed into the bloodstream and becomes available for therapeutic action. Several factors can significantly influence the bioavailability of tablets. Understanding and optimizing these factors are essential in designing effective and…

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Tablets

How are medical devices tested for mechanical performance?

Posted on August 10, 2023August 2, 2023 By Admin

Testing of Medical Devices for Mechanical Performance Mechanical performance testing is a crucial aspect of ensuring the safety and efficacy of medical devices. These tests assess how well a device functions mechanically and how it withstands various physical stresses and forces it may encounter during use. Here are the key steps involved in testing medical…

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Medical Devices

What is the significance of disintegration time in tablet formulation?

Posted on August 10, 2023August 5, 2023 By Admin

Significance of Disintegration Time in Tablet Formulation In the field of pharmaceutical manufacturing, the disintegration time of tablets is a critical parameter that directly influences the drug’s efficacy, bioavailability, and patient compliance. Disintegration time refers to the period it takes for a tablet to break down into smaller particles and disperse in a solution, typically…

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Tablets

How are capsule formulations developed for pediatric use?

Posted on August 10, 2023July 31, 2023 By Admin

Development of Capsule Formulations for Pediatric Use Developing capsule formulations for pediatric use requires careful consideration of various factors to ensure the safety, efficacy, and acceptability of the medication for children. Pediatric formulations need to be age-appropriate, easy to administer, and palatable. Here’s a step-by-step guide to the development of capsule formulations for pediatric use:…

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Capsules (Hard & Soft Gelatin)

How is the tablet’s porosity controlled during production?

Posted on August 10, 2023July 31, 2023 By Admin

Controlling Tablet Porosity During Production Tablet porosity refers to the amount of empty space or voids within a tablet. Controlling tablet porosity is essential in tablet manufacturing to ensure consistent drug content, disintegration, and dissolution properties. The porosity of tablets can be influenced by several factors during the production process. Here are some key methods…

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Tablets

What are the challenges in manufacturing medical devices with electronics and software components?

Posted on August 9, 2023August 2, 2023 By Admin

Challenges in Manufacturing Medical Devices with Electronics and Software Components The integration of electronics and software components in medical devices has significantly advanced healthcare capabilities, enabling enhanced diagnostics, data monitoring, and treatment options. However, this integration also introduces several challenges in the manufacturing process. Here are the key challenges faced in manufacturing medical devices with…

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Medical Devices

What are the critical factors affecting the stability of ointments, creams, and gels?

Posted on August 9, 2023August 2, 2023 By Admin

Critical Factors Affecting the Stability of Ointments, Creams, and Gels The stability of ointments, creams, and gels is essential to ensure their effectiveness, safety, and shelf life. Various factors can impact the stability of these topical dosage forms, leading to changes in appearance, texture, drug content, and efficacy. Here are some critical factors that can…

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External Preparations

How are injectables formulated for targeted drug delivery?

Posted on August 9, 2023August 2, 2023 By Admin

Formulation Strategies for Targeted Drug Delivery in Injectables Targeted drug delivery in injectables aims to deliver medications selectively to specific tissues or cells while minimizing systemic exposure and reducing side effects. To achieve targeted drug delivery, various formulation strategies are employed in injectable products. Here are some common approaches: 1. Nanoparticles and Liposomes Nanoparticles and…

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Parenteral Drug Manufacturing

What are the different types of capsule filling machines used in the industry?

Posted on August 9, 2023July 31, 2023 By Admin

Different Types of Capsule Filling Machines Used in the Industry Capsule filling machines are essential equipment in the pharmaceutical industry for filling empty capsules with active pharmaceutical ingredients (APIs) and other formulations. Different types of capsule filling machines are available, each designed to meet specific production requirements and capsule sizes. Here are the main types…

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Capsules (Hard & Soft Gelatin)

What are the different types of tablet disintegration tests?

Posted on August 9, 2023July 31, 2023 By Admin

Different Types of Tablet Disintegration Tests Tablet disintegration tests are crucial quality control tests used to assess the time it takes for a tablet to break down into small particles in a standardized disintegration medium. Disintegration testing is essential to ensure that the tablet disintegrates rapidly and completely after ingestion, allowing for proper drug release…

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Tablets

Posts pagination

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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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