Tips for GLP Guidelines

In Good Laboratory Practices in pharma (GLP), routine maintenance of laboratory equipment is essential for ensuring accuracy, reliability, and regulatory compliance. Proper maintenance reduces the risk of equipment failure, enhances operational efficiency, and supports GLP compliance in pharmaceutical laboratories. This article provides a step-by-step guide to conducting routine maintenance for GLP equipment, highlighting best practices and key considerations.
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In Good Laboratory Practices in pharma (GLP), equipment validation is a critical process that ensures laboratory instruments are functioning accurately and consistently. Proper validation supports GLP compliance in pharmaceutical laboratories, enhances data reliability, and meets regulatory standards. This article explores the key GLP guidelines for equipment validation and their importance in non-clinical studies.
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In Good Laboratory Practices in pharma (GLP), test system facilities play a crucial role in ensuring the reliability, accuracy, and compliance of non-clinical studies. These facilities are designed to house and manage test systems, such as animals, plants, or microorganisms, under controlled conditions. Proper management of GLP-compliant test system facilities is essential for maintaining data integrity and achieving GLP compliance in pharmaceutical laboratories. This article explores the key roles and best practices for test system facilities in GLP studies.
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Designing animal facilities that comply with Good Laboratory Practices in pharma (GLP) is crucial for maintaining animal welfare, ensuring data reliability, and achieving GLP compliance in pharmaceutical laboratories. Proper facility design supports the ethical conduct of studies and meets regulatory standards. This article provides 10 practical tips for creating GLP-compliant animal facilities that are efficient, safe, and compliant with international guidelines.
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Equipment qualification is a critical requirement under Good Laboratory Practices in pharma (GLP). It ensures that laboratory instruments and equipment function as intended, providing accurate and reliable results. Adhering to GLP compliance in pharmaceutical laboratories, equipment qualification involves several phases, from installation to performance validation. This article provides a step-by-step guide to performing equipment qualification as per GLP standards.
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Proper maintenance of laboratory equipment is a critical aspect of Good Laboratory Practices in pharma (GLP). Well-maintained equipment ensures accurate and reliable results while supporting GLP compliance in pharmaceutical laboratories. In this FAQ, we address the key GLP requirements for laboratory equipment maintenance and how to meet them effectively.
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In Good Laboratory Practices in pharma (GLP), selecting the right equipment is crucial for ensuring accurate results, operational efficiency, and GLP compliance in pharmaceutical laboratories. Proper equipment selection reduces errors, enhances data reliability, and minimizes non-compliance risks. This article provides a comprehensive list of do’s and don’ts for selecting equipment in GLP-compliant laboratories.
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Environmental controls are essential for maintaining Good Laboratory Practices in pharma (GLP) and ensuring the reliability of non-clinical studies. Properly managing environmental parameters such as temperature, humidity, and ventilation is critical for achieving GLP compliance in pharmaceutical laboratories. This article outlines the key steps and best practices for managing environmental controls in GLP-compliant facilities.
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In Good Laboratory Practices in pharma (GLP), a well-organized test system facility is essential for ensuring the accuracy, reliability, and compliance of non-clinical studies. A GLP-compliant facility minimizes errors, supports data integrity, and meets regulatory requirements. This step-by-step guide outlines the process of setting up a test system facility for GLP compliance in pharmaceutical laboratories.
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A well-designed laboratory facility is fundamental to achieving Good Laboratory Practices in pharma (GLP) compliance. Facility design directly impacts the accuracy, integrity, and safety of non-clinical studies conducted in GLP-compliant pharmaceutical laboratories. This article explores the essential design requirements for laboratories to ensure adherence to GLP guidelines.
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Multi-site studies are becoming increasingly common in Good Laboratory Practices in pharma (GLP) as research expands across geographic locations and specialized facilities. However, ensuring accountability in multi-site studies presents unique challenges. Proper systems and processes are essential to maintain GLP compliance in pharmaceutical laboratories and ensure that all sites adhere to the same rigorous standards. This article outlines strategies for maintaining accountability across multiple sites in GLP studies.
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In Good Laboratory Practices in pharma (GLP), the Study Director is the single point of control responsible for ensuring the integrity and compliance of non-clinical studies. Documenting decisions made by the Study Director is critical for achieving GLP compliance in pharmaceutical laboratories. Proper documentation supports transparency, traceability, and regulatory readiness. This article outlines best practices for documenting Study Director decisions under GLP guidelines.
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