Introduction In today’s highly regulated pharmaceutical industry, data integrity, traceability, and compliance are no longer optional. Pharmaceutical companies are increasingly adopting LIMS software (Laboratory Information Management System) to streamline laboratory operations, ensure FDA compliance, and maintain audit-ready documentation. This article explains what LIMS software is, its pricing in the USA, key features pharma companies need, and how it supports FDA 21 CFR Part 11 and GMP compliance. What Is LIMS Software in the Pharmaceutical Industry? A LIMS (Laboratory Information Management System) is a software solution designed to manage laboratory samples, test data, workflows, instruments, and compliance records. For pharmaceutical companies, LIMS helps in: Managing QC and QA data Tracking samples from receipt to final approval Maintaining data integrity (ALCOA++) Supporting FDA and regulatory audits Why Pharmaceutical Companies Need LIMS Software Pharma laboratories han...