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Industry

Pharma and APIs

Batch records, deviations and stability data that stand up to an inspection without three weeks of preparation.

What we hear

  • Regulatory inspections with little notice
  • Batch record evidence spread across paper and systems
  • Yield variation between campaigns that nobody can fully explain

Where we usually start

  • Batch genealogy in one place

    Trace a finished batch back through intermediates and raw materials without reassembling it by hand each time.

  • Deviation and CAPA visibility

    See open deviations by age and area, so the backlog is managed rather than discovered at audit.

  • Campaign yield comparison

    Compare like-for-like campaigns to find which process conditions actually move yield.

Target: cut audit preparation from weeks to days by assembling evidence from source data. [FIGURE TO CONFIRM]

Start with one number worth moving.

An hour on a call gets you a written view of where your data stands, whether or not you work with us.

Book a discovery call