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  • GLP Guidelines

What Are the Duties of Principal Investigators in GLP Studies?

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What Are the Duties of Principal Investigators in GLP Studies? Understanding the Role of Principal Investigators in GLP Studies Introduction In Good Laboratory Practices in […]

  • Tablet Manufacturing

Preventing Tablet Capping in Formulation Stages

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Preventing Tablet Capping in Formulation Stages Troubleshooting and How-To Guide: Preventing Tablet Capping in Formulation Stages Overview: Tablet capping is a common issue in pharmaceutical […]

  • Tablet Manufacturing

Optimizing Moisture Content in Direct Compression Tablets

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Optimizing Moisture Content in Direct Compression Tablets Expert Guide to Optimizing Moisture Content in Direct Compression Tablets Why is Moisture Content Important in Direct Compression […]

  • GLP Guidelines

How to Ensure Adequate Training for GLP Study Personnel

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How to Ensure Adequate Training for GLP Study Personnel Comprehensive Guide to Training GLP Study Personnel Introduction In Good Laboratory Practices in pharma (GLP), proper […]

  • Drug Discovery

Using Alternative Models in Preclinical Studies

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Using Alternative Models in Preclinical Studies How to Use Alternative Models in Preclinical Studies Exploring Non-Animal Models to Improve Drug Development Alternative models in preclinical […]

  • Tablet Manufacturing

Achieving Consistency in Tablet Weight During Formulation Development

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Achieving Consistency in Tablet Weight During Formulation Development Step-by-Step Guide: Ensuring Consistent Tablet Weight in Formulation Development Overview: Consistency in tablet weight is a critical […]

  • Aerosol Formulations

Improving Propellant Stability in Combination Formulations

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Improving Propellant Stability in Combination Formulations Expert Guide to Enhancing Propellant Stability in Aerosol Formulations What Are Combination Formulations in Aerosols? Combination formulations in aerosol […]

  • Tablet Manufacturing

How to Conduct Risk Assessments in Tablet Manufacturing

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How to Conduct Risk Assessments in Tablet Manufacturing Step-by-Step Guide to Conducting Risk Assessments in Tablet Manufacturing What is Risk Assessment in Tablet Manufacturing? Risk […]

  • GLP Guidelines

Do’s and Don’ts for Managing Personnel in a GLP-Compliant Lab

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Do’s and Don’ts for Managing Personnel in a GLP-Compliant Lab Effective Personnel Management in GLP-Compliant Laboratories Introduction Personnel management is a cornerstone of Good Laboratory […]

  • Tablet Manufacturing

Role of Functional Polymers in Extended Release Tablets

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Role of Functional Polymers in Extended Release Tablets Research & Trends: The Role of Functional Polymers in Extended Release Tablets Overview: Extended-release (ER) tablets are […]

  • Tablet Manufacturing

Preventing Crosslinking in Modified Release Tablets

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Preventing Crosslinking in Modified Release Tablets FAQs on Preventing Crosslinking in Modified Release Tablets What is Crosslinking in Modified Release Tablets? Crosslinking refers to the […]

  • Tablet Manufacturing

Designing Bilayer Tablets for Complex Release Patterns

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Designing Bilayer Tablets for Complex Release Patterns Step-by-Step Guide: Designing Bilayer Tablets for Complex Release Patterns Overview: Bilayer tablets have emerged as an innovative solution […]

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