Ultimate Guide
Optimize Batch Records with Pharma Manufacturing Software
You will learn how to:
- Connect all pharma manufacturing business units to gain more insight into all areas of the operation.
- Resolve pharma manufacturing production bottlenecks by making data-driven comparisons between sites, shifts, teams, and more.
- Ensure compliance by mastering regulatory GMPs.
About This Asset
This guide details how pharmaceutical manufacturers are addressing production lapses and compliance issues by digitizing their operations. Digital transformation in pharma manufacturing is essential to resolving product shortages and remaining relevant in today’s market.
Trusted By
Why Digitization in Manufacturing Is Critical
Pharma Product Shortages Are Alarmingly High
A digitized manufacturing execution system (MES) enables you to capture pharma manufacturing data and insights to reduce errors, deviations, and corrective actions/preventive actions (CAPAs).
Blind Spots Are Common in Manufacturing Processes
A digitized MES gives pharma manufacturing companies full visibility of production. View performance data between sites, shifts, teams, and more.
Paper Batch Records Often Stall cGMP Compliance
GMPs continue to evolve. Pharma manufacturing companies need to adopt electronic batch records (EBR) to stay current with the updated guidelines.
Shorten Your Time to Market
Digitizing
pharma manufacturing speeds up quality reviews and product releases.
Read the Ultimate Guide