GMP (Good Manufacturing Practice) and GLP (Good Laboratory Practice) are both quality assurance systems that are crucial in the pharmaceutical manufacturing industry. While they share some similarities, there are also notable differences between the two concepts. Standards: 1. GMP: GMP focuses on ensuring that pharmaceutical products are consistently produced and controlled according to quality…
USP <711> contains a couple references to pooled sampling for dissolution. What is pooled sampling and when is it appropriate? What risks are there with pooled sampling? Pooled sampling is a procedure where each sample from a dissolution time point is combined into a single sample. Pooled sampling is only done for immediate-release dosage…
Achieve cost-effectiveness and operational efficiency in pharmaceutical packaging with optimized processes and streamlined operations. Optimize packaging materials and strategies to reduce costs without compromising quality or safety. Enhance efficiency through advanced automation technologies and inventory management systems. Optimizing Packaging Processes Streamlining the packaging processes is crucial for pharmaceutical companies to ensure cost-effectiveness and operational…
Prerequisites is usually a checklist which is sent to the Receiving Laboratory which in most of the cases is the Quality control laboratory of the manufacturing. This checklist is prepared by the Department or the team which is involved in the method validation/verification/transfer activity and contains all the things which are required and needed…
Advanced materials and technologies play a crucial role in the field of pharmaceutical packaging. These innovative solutions enhance the safety, security, and efficiency of medication delivery, ensuring optimal patient care. Smart And Intelligent Packaging Integration of sensors and electronic devices in packaging to monitor various factors like temperature, moisture, and light exposure. …
1. Start by identifying the areas in the storage facility that need to be temperature mapped. This could include refrigerators, freezers, cold rooms, or any other specific areas where temperature control is critical. 2. Determine the appropriate temperature range for each area based on the specific requirements of the stored items. This could vary…
When it comes to pharmaceuticals, the focus often centers on the active ingredients that bring relief and healing. However, the less-discussed but equally important components in drugs are known as excipients. Excipients are essential for various reasons, including drug stability, bioavailability, and even patient safety. In the realm of injectable medications, the role of excipients…
One major criterion for selecting the QC dissolution method should be its discriminatory power to show changes in the critical attributes of the release mechanism of the chosen formulation. The discriminatory power is the ability of a test procedure to discriminate between batches manufactured with different critical process parameters and /or critical material attributes…
