What we do
Pre-construction
Commissioning
Post handover
Every certificate, test record and signature captured as the work happens. So turnover packs build themselves and commissioning and qualification starts on schedule.
Chasing contractors for documents takes up the week, and commissioning cannot start until the pack is accepted. EIDA changes the order. Every certificate, test record and signature is captured and checked as the work is done. Once the build is complete, the pack is complete.
Proof First-pass turnover pack rejection runs at 40 to 60 per cent without a dedicated system.
EIDA puts them all on the drawing. You see what is done, what is outstanding and what is about to slip, while there is still time to act. Documentation delays of four to twelve weeks are common across the industry. You find out about yours early enough to do something.
One week of delayed operational readiness can cost between $1 million and $5 million. Around a third of what inspectors write up at a pharma facility relates to documentation. EIDA gives you a verified record that holds up under inspection years after the contractors have gone, and the same standard on every project you run.
Everything is online. It's easy to check, easy to review, easy to approve, easy to ask for more detail.
EIDA is used on pharmaceutical builds for Merck and Pfizer, built from sixteen years of processes developed with the trade contractors who use them, and certified to 21 CFR Part 11, EU GMP Annex 11.
After handover The record stays on. It becomes the facility's working memory, for the next audit, the next inspection and the next expansion.
