SOLUTIONS · PHARMA

100% inspection, with a record of every unit.

Regulated lines need consistent inspection and complete documentation. Human inspection varies by inspector, shift and fatigue.

WHAT'S AT STAKE

Every unit inspected. Every result documented.

RISK
USP <790> expects 100% inspection of injectable units, with defective units removed.
SOURCE · USP <790>
RISK
Results must be documented and out-of-spec results investigated.
SOURCE · USP <790> / cGMP PRACTICE
RISK
Human inspection performance varies across inspectors and shifts.
SOURCE · USP <1790>
WHAT VIAI CATCHES
malformed
Malformed tablet
missing-tablet
Missing tablet
code-illegible
Batch code legibility
tamper
Tamper seal
WHERE IT SITS ON YOUR LINE

Three typical stations.

01
Blister forming and sealing
Fill, tablet shape, missing units.
02
Coding check
Batch code and expiry legibility.
03
Final pack
Tamper seal and carton integrity.
HOW VIAI FITS

Your problems, and the product that solves each one.

PROBLEM
Documentation
SOLUTION
Image, verdict and model version for every unit.
VIAI Cloud →
PROBLEM
Validation before go-live
SOLUTION
Run the detector on saved images and keep the report.
VIAI Simulator →
PROBLEM
Consistency across shifts
SOLUTION
The same verdict logic on every unit, every shift.
VIAI Edge →
PROBLEM
Controlled change
SOLUTION
Every model release checked, approved and recorded.
VIAI VisionLab →

See it on your part.

20 minutes. Bring a sample. Leave with a working detector.

[email protected]
Plants in Canada and the US. Reply within one business day.