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October 17, 2024

5 Key Benefits of Biopharmaceutical Consulting

Improve your pharmaceutical product’s chances of success by engaging a biopharmaceutical consultant. These specialists offer essential expertise in drug development, clinical trial design, regulatory compliance, and market strategy. Their deep industry knowledge helps you make informed decisions, avoiding costly pitfalls, and accelerating your path to market. By benefiting from their […]
October 23, 2024

Understanding QP Certification & Batch Release

Quality, safety, and efficacy are core tenets of pharmaceutical manufacturing. One critical component of this assurance process is batch release. This is a meticulously controlled procedure overseen by a Qualified Person (QP). Our blog aims to elucidate the nuances of QP certification and batch release within the European Union (EU), […]
January 6, 2025

Best practices for lab-to-plant technology transfers in drug substance manufacturing

In the pharmaceutical industry, the successful transition of a drug substance from the controlled environment of the laboratory to large-scale production at a manufacturing plant is critical. This process, known as technology transfer, ensures that the product maintains its quality, integrity, and compliance with regulatory standards at every scale. At […]
January 11, 2025

How Quality Assurance Consulting Helps Prevent Compliance Issues

Regulatory compliance defines success in biopharmaceuticals and medical devices. A missed step can lead to recalls, financial losses, or patient harm. Quality assurance (QA) consultants, like DSI, help companies tackle these risks. Our expertise strengthens compliance strategies, mitigates issues, and boosts operational efficiency. Learn how quality and compliance consulting secures […]