Caliber Technologies

Investigating a discrepancy on paper means going back through the batch record page by page. CaliberBRM logs every activity with the operator’s name and a timestamp, so the full batch history is in one place. Caliber has been building software for pharma manufacturers since 2001. See how CaliberBRM tracks each step of a batch.

When a batch record doesn’t match how a product is made, operators add notes and QA follows up on each one. CaliberBRM lets you configure reusable templates around each product and process. Pharma manufacturers in 16+ countries already work with Caliber. Explore how templates are set up in CaliberBRM.

Every instrument result typed into a sample record by hand needs a second check. CaliberLIMS pulls results straight from your instruments into the right sample record. It can save more than 30% of an analyst’s time. Explore how CaliberLIMS connects to your instruments.

After production, the batch waits while QA checks every record entry. CaliberBRM flags discrepancies as each step is recorded, so batches reach release sooner. Approvals still run through electronic signatures built to support 21 CFR Part 11. Explore how review by exception works in CaliberBRM.

A lab result on paper can take hours to trace back through logbooks and printouts. CaliberLIMS keeps every transaction in the audit trail, so a result’s complete history stays in one record. It has supported pharma labs for 20+ years and is designed for 21 CFR Part 11 and EU Annex 11. Learn how CaliberLIMS keeps each result traceable.

Moving batch records off paper can look like a project that will take months. CaliberBRM gets you up and running in 60 days, with a stage-wise rollout that limits disruption on the shop floor. Caliber has 25 years of pharma implementations and offices in the US and EU. See how to get started with CaliberBRM.