Ensuring Drug Quality and Safety: Pharmaceutical LIMS Best Practices
Ensuring drug quality and patient safety is at the heart of pharmaceutical manufacturing, where strict regulatory frameworks like FDA 21 CFR Part 11 and ISO 17025 are non-negotiable. As operations scale and complexity increase, so does the need for robust digital infrastructure. A Pharmaceutical Laboratory Information Management System (LIMS) has become indispensable in this environment, offering automation, data integrity, and end-to-end compliance. By streamlining quality control and providing real-time oversight, LIMS empowers pharmaceutical companies to meet regulatory demands efficiently and consistently. In this blog, we explore how Pharmaceutical LIMS enhances drug safety, outline best practices for implementation, and highlight the essential features to look for in an effective solution.
