Design Specifications (DS) vs. User Requirements Specifications (URS) in a GMP Environment

In Good Manufacturing Practices (GMP) environment, ensuring that systems and equipment meet regulatory standards is critical. Two pivotal documents that play significant roles in this process are the Design Specification (DS) and the User Requirements Specification (URS). While both are essential, they serve distinct purposes and are developed at different stages of a project. What…

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Overview of Periodical Review of Equipment in GMP Environments.

In the dynamic field of Good Manufacturing Practices (GMP), ensuring the integrity, efficiency, and compliance of equipment is a requirement. This article looks into the essential aspects of periodical equipment reviews within GMP environments, highlighting their significance, processes, and outcomes. The Necessity of Periodical Equipment Reviews Regular reviews are crucial for maintaining equipment functionality and…

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