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SSI Visual Inspection

SSI VIB Series
Manual Visual Inspection Booths

‘The VIB Series: configurable inspection booths with calibrated multi-LUX lighting, compliant with USP <1790>, EU GMP Annex 1, and 21 CFR Part 211

Trusted by
90+ Drug Manufacturers Globally

SSI Visual Inspection Booths - Designed for Regulatory Compliance

Regulatory guidance has moved from just a white and black background to necessitating Ensuring consistency, operator comfort, and accurate defect detection across container types and product profiles.

The VIB Series is engineered from the ground up to meet the lighting and ergonomic requirements of USP <1790> and EU Annex 1. Every unit ships with Settable light System with diffuser(2,000– 10,000+LUX) and a qualification documentation package.

Watch our Visual Inspection Booths and see the features in action.

Dual Light System

Stage 1: 2,000-3,750 LUX (general inspection)
Stage 2: 8,000-10,000 LUX (Difficult to inspect containers such as amber vials)

Automated Timing

Dual-sensor system ensures 5-second inspection per background (black & white) with audio/visual alerts


Eye Protection

Auto eye rest function with adjustable intervals (15-30 mins) and stabilization timer.


Stabilization Mode

Programmable warm-up period (5/10/15 mins) ensures consistent light output

Ergonomic Design

15° angled viewing stage reduces neck strain with height-adjustable stand.

Audit Trails

Optional 21 CFR Part 11 electronic records for full audit trails.


Feature Comparison Summary

VIB-50 to VIB-300 — scalability for production and regulated pharma exports

Feature

VIB-50 (Basic)

VIB-100 (Standard)

Most Popular

VIB-200 (Advanced)

VIB-300 (Smart)

Construction & Design

SS 304 matte-finish, ergonomic design

Settable Light System with Diffuser
2,000–10,000+ LUX

Inspection Backgrounds
Dual non-reflective matte black & white

Compatible Products  *
Vials, ampoules, bottles, prefilled syringes, cartridges

Lighting Type  *
Low-power LED for long life, minimal maintenance

Inspection Alert System
5-sec timer + dual hand-detection sensors

–

Auto Eye-Rest / Stabilization Timer
Red/green tower lamp; configurable alert or power interlock

–

Light Stabilisation Warm-up
Programmable 5/10/15 min

–

PLC + HMI Control
Customisable logic per URS

–

Password-Protected

–

Dimmer Control

–

–

Light Measurement Sensor

–

–

21 CFR Part 11 Compliance

–

–

–

Audit Trails & E-Signature
Secure login, e-signature, timestamped logs

–

–

–

Data Logging & Export

–

–

Partial

Full

100% Verification of I/Os, Alarms & Interlocks
Per IQ and OQ

–

Documentation
GA Drawing, Electrical Drawing, Test & Calibration Certs, FDS, IQ, OQ

*

Best Use Case

Production and QA

Production and QA

Production and QA

Regulated Export Pharma

Lead Time

2-4 weeks

4-6 weeks

4-6 weeks

4-6 weeks

Available customizations

Table Top / Folded Legs

Rejection Tray

Arm Rest

Magnification Glass

All SSI VIB Models Are Available in Customized Configurations

Share your URS and we will configure a booth to match your exact production requirements.

Ready to Place an Inquiry?

Regulatory Compliance Deep-Dive

Parameters that determine the audit readiness of your inspection process as per USP <1790>

USP ‹1790› Compliant Visual Inspection

Controlled Illumination
  • Minimum 2,000 lux at the point of inspection for clear glass containers — the hard regulatory floor
  • Upper range of 2,000–3,750 lux for routine inspection, harmonized with European Pharmacopoeia
  • Up to 10,000 lux or higher for amber glass or translucent plastic containers
  • Light must be diffuse and even across the defined inspection zone
  • High-frequency ballasts required to eliminate flicker-induced inspector fatigue
  • LED sources accepted as a stable, heat-free alternative
  • Lux must be periodically monitored with a documented action limit to prevent sub-limit inspection
  • Both backgrounds are required to detect the full spectrum of light and dark defects 
  • All backgrounds must be matte/non-glossy to prevent reflection interference 
  • Inspection against each background: minimum 5 seconds per background (as per USP ‹790›)

USP ⟨790⟩ establishes a reference inspection time of 10 seconds per container: 5 seconds against the black background, 5 seconds against the white. This is not an arbitrary number. It reflects the time required to generate and observe particle motion, which is the primary mechanism by which the human visual system detects foreign material in solution.

USP ⟨1790⟩ notes that recording the time spent inspecting each batch and calculating a nominal inspection rate is good practice for demonstrating that timing remained within established limits. Without a mechanism to enforce this, inspection time becomes a function of individual pace — and Probability of Detection becomes an unrepeatable variable.

  • Adjustable seating, ergonomic positioning and product flow to minimize repetitive-motion injury 
  • Mandatory documented breaks at minimum every 60 minutes to maintain detection performance 
  • Breaks satisfied by short rest, meal break, or rotation to non-inspection tasks
  • Inspection rate is a critical parameter: must be controlled, documented, included in qualification 
  • Rate deviations must be addressed: inspection outside the qualified rate range is non-compliant
  • Reduced ambient lighting to eliminate distraction from extraneous reflections 
  • Temperature and humidity controlled for inspector comfort and performance consistency 
  • No uncontrolled daylight ingress: windows require special management to prevent variable ambient conditions 

Frequently Asked Questions

How do I choose between the VIB-50, VIB-100, VIB-200 and VIB-300?

All models have the basic features required for compliance with USP <1790> i.e. black and white background and diffused light from 2,000 to 10,000 lux. The VIB-50 is positioned as an entry model; VIB-100 for typical production/QA have the 5 second inspection alert and eye stabilization time ; VIB-200 adds dimmer control and light measurement; and VIB-300 adds 21 CFR Part 11 functionality, audit trails and e-signatures. VIB-100 is our most popular model with the automation features required in an audit-ready setup. VIB- 200 is for facilties who require a specific lux range and VIB-300 is for plants requiring 21 CFR Part 11 functionality.

Yes. SSI reviews the submitted URS, confirms feasibility, provides an working drawing for sign-off and then issues a formal proposal against the agreed specification.

Yes. SSI can arrange virtual demonstrations of specific booth models, including its 21 CFR Part 11-capable model. Onsite paid demos can also be arranged for interested customers.

Yes. SSI provides technical documentation support for URS development, standard IQ/OQ documentation and a PQ template for the customer’s performance qualification.

Yes. SSI can configure inspection booths for difficult-to-inspect formats. USP <1790> provides guidance for lux levels between 8,000 and 10,000 lux for DIP containers and all our booth models support the same.

Yes. SSI can help design, develop and manufacture semi-automated visual inspection machines for vials and pre-filled syringes.

Order Process

1

Select Your Model

Based on site requirements and inspection type

2

Share Your Customization

Tabletop or folding legs, rejection tray, magnification glass, carrying handle, or any other custom request

3

Receive & Approve Quotation

SSI shares a detailed proposal; customer raises PO

4

Sign Off on Specifications

SSI confirms your User Requirement Specification (URS) to lock in all technical details

5

Drawing Approval

SSI shares working drawings for your review and sign-off

6

Delivery & Shipping

New to MVI systems?

SSI provides a draft URS template to help you get started, and our team is available for a technical consultation call at any stage of the process. 

Get in Touch

Ready to Place an Inquiry?

Let’s make your Visual Inspection Program Audit – ready

Email

info@ssiexport.com

Phone

+91 9040 479 033

WhatsApp

+91 9040 479 033

Know more

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P3: MVI Booth Form (#6)