Manual visual inspection plays a crucial role in upholding product integrity, patient safety, and regulatory...
Ensuring the safety and quality of injectable drugs requires rigorous standards in facility design, equipment...
Semi-automated visual inspection (SAVI) bridges the gap between fully manual and fully automated inspection systems, combining the strengths of human oversight with the consistency and efficiency of automation.
When particulate matter is detected in sterile injectable products, manufacturers must take swift, structured steps...
FDA Injectable Drug Recall Notices: Interactive Chart
Semi-automated visual inspection (SAVI) bridges the gap between fully manual and fully automated inspection systems, combining the strengths of human oversight with the consistency and...
Manual visual inspection plays a crucial role in upholding product integrity, patient safety, and regulatory compliance. Let's dive into the details of this essential quality...
Ensuring the safety and quality of injectable drugs requires rigorous standards in facility design, equipment selection, and inspection processes. This guide explores the key cGMP...
When particulate matter is detected in sterile injectable products, manufacturers must take swift, structured steps to investigate and assess potential risks. This guide covers essential...
FDA Injectable Drug Recall Notices: Interactive Chart
Ensuring compliance with Section 501 of the FD&C Act is vital for maintaining the safety, quality, and efficacy of pharmaceutical products. Strict adherence to environmental...
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Semi-automated visual inspection (SAVI) bridges the gap between fully manual and fully automated inspection systems, combining the strengths of human oversight with the consistency and efficiency of automation.
Manual visual inspection plays a crucial role in upholding product...
Ensuring the safety and quality of injectable drugs requires rigorous...
When particulate matter is detected in sterile injectable products, manufacturers...
Ensuring compliance with Section 501 of the FD&C Act is...
Injectable products are a type of pharmaceutical formulation designed to...
Properly designed defect test sets are essential for qualifying inspectors...
Semi-automated visual inspection (SAVI) bridges the gap between fully manual and fully automated inspection systems, combining the strengths...
Manual visual inspection plays a crucial role in upholding product integrity, patient safety, and regulatory compliance. Let's dive...
Ensuring the safety and quality of injectable drugs requires rigorous standards in facility design, equipment selection, and inspection...
When particulate matter is detected in sterile injectable products, manufacturers must take swift, structured steps to investigate and...
Semi-automated visual inspection (SAVI) bridges the gap between fully manual and fully automated inspection systems, combining the strengths of human oversight with the consistency and...
Manual visual inspection plays a crucial role in upholding product integrity, patient safety, and regulatory compliance. Let's dive into the details of this essential quality...
Ensuring the safety and quality of injectable drugs requires rigorous standards in facility design, equipment selection, and inspection processes. This guide explores the key cGMP...
When particulate matter is detected in sterile injectable products, manufacturers must take swift, structured steps to investigate and assess potential risks. This guide covers essential...
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FDA Injectable Drug Recall Notices: Interactive Chart
The affected batches were inadvertently released to the market prior to the completion of the required acceptance activities for embedded particulate matter which may result in leakage. To date, there have been no customer complaints received and there have been no reports of serious injury...
Par Pharmaceutical, Inc. has voluntarily recalled one lot of Treprostinil Injection 20mg/20mL (1mg/mL) to the consumer level. The product was recalled due to the potential for the presence of silicone particulates in the product solution.
The recall was initiated due to the potential for presence of glass particulate matter, identified during product inspection.
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