February 2023 - Pharmaceutical Guidelines

Hold Time Study Report for Dirty Equipment in the Injection Ampoule Section

A hold time study report is an essential part of the quality control process that determines the maximum time for which a product can be held or stored under specified conditions. In the case of dirty equipment in the injection ampoule section, this study is critical for ensuring that the equipment does not introduce contamination […]

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Tips For Effective Internal Audit

Quality Assurance

The pharmaceutical industry is a highly regulated sector that requires strict adherence to laws and regulations to ensure the safety and efficacy of its products. One of the key mechanisms for ensuring compliance and mitigating risk is through effective internal audits. Here are some tips to help ensure your internal audits are as effective as

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Material management in a pharmaceutical warehouse department.

Quality Assurance

Material management in a pharmaceutical warehouse department. Read More »

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