Pharmaceutical and biotech
Batch manufacture where the electronic batch record, signature, deviation handling and audit trail carry regulatory weight, and release time is a commercial constraint.
Industries
Built for regulated manufacturing
SiBR was designed primarily for life sciences customers, where the record is as regulated as the product — and built on process patterns that hold across industries.
Medical devices
Device history records, controlled assembly sequence and traceability of components and equipment through production.
Food, beverage and nutrition
Recipe control, allergen and changeover discipline, and traceability from raw material through to the shipped lot.
Speciality and fine chemicals
Process orders with tight parameter control, where deviations need to be visible while the batch is still in progress.
Evidence
Proven in regulated manufacturing
Enterprise EBR live in nine months
A European manufacturer replaced its existing electronic MES with SiBR across packaging to harmonise global operations on SAP. Because SiBR’s master-data model needs no interfaces, the plant team began authoring master batch records after about a week of training. The fully integrated enterprise solution went live in nine months, with the second production batch completed within days — and operators’ first reaction was “this is SAP? It is much faster than our old system.”
More on request
Further references across pharmaceutical, biotech and process manufacturing are available under NDA. Ask us on a call and we will connect you with a comparable site.
Does your process look like this?
Fifteen minutes on a call is usually enough to tell whether SiBR fits.