Nexgensis TechnologiesNexgensisTechnologies

OPS IQ Product Suite

Ten products. One integrated platform.

Start where the pain is greatest and expand without re-integration. Every product runs on OPS IQ — one data model, one security model, one validation package.

10
Enterprise products
4
Architecture layers
1
Shared data model
1
Validation package
OPS IQ · eQMS · CAPA
Nexgensis OPS IQ eQMS · CAPA workspace

Product catalogue

Start with one. Grow into all ten.

eQMS workspace in Nexgensis OPS IQ
Quality

eQMS

Enterprise Quality Management

Unify deviations, CAPA, change control, complaints and audits in one validated, workflow-driven quality system.

  • Deviation & CAPA
  • Change Control
  • Audit Management
  • Risk & Complaints
Explore eQMS
LIMS workspace in Nexgensis OPS IQ
Laboratory

LIMS

Laboratory Information Management

Sample lifecycle, stability, instrument integration and out-of-specification handling with full data integrity.

  • Sample Lifecycle
  • Stability Studies
  • Instrument Interfacing
Explore LIMS
ELN workspace in Nexgensis OPS IQ
Laboratory

ELN

Electronic Lab Notebook

Structured, reviewable experiment records that replace paper notebooks without slowing scientists down.

  • Experiment Templates
  • Review & Approve
  • Reagent Traceability
Explore ELN
eBMR workspace in Nexgensis OPS IQ
Manufacturing

eBMR

Electronic Batch Manufacturing Records

Right-first-time execution with in-line checks, exception-based review and dramatically faster batch release.

  • Recipe Authoring
  • In-line Verification
  • Review by Exception
Explore eBMR
DMS workspace in Nexgensis OPS IQ
Quality

DMS

Document Management

Controlled SOP lifecycle from authoring to periodic review, with e-signatures and automated distribution.

  • SOP Lifecycle
  • e-Signature
  • Version Control
Explore DMS
LMS workspace in Nexgensis OPS IQ
Quality

LMS

Training Management

Role-based curricula tied directly to SOP revisions, so training compliance never drifts from documents.

  • Job Role Curricula
  • Read & Understood
  • Assessments
Explore LMS
eLogs workspace in Nexgensis OPS IQ
Manufacturing

eLogs

Electronic Logbooks

Replace every paper logbook — equipment usage, cleaning, environmental monitoring — with ALCOA++ records.

  • Equipment Usage
  • Cleaning Logs
  • EM Records
Explore eLogs
Enterprise Asset Management workspace in Nexgensis OPS IQ
Manufacturing

Enterprise Asset Management

Assets, Calibration & Maintenance

Preventive maintenance, calibration schedules and qualification status for every GxP-critical asset.

  • Calibration Schedules
  • Preventive Maintenance
  • Breakdown Tracking
Explore Enterprise Asset Management
APQR workspace in Nexgensis OPS IQ
Analytics

APQR

Annual Product Quality Review

Automated data aggregation and trending that turns a twelve-week reporting exercise into a few days.

  • Automated Aggregation
  • Trend & Cpk Analysis
  • Review Workflow
Explore APQR
AI Analytics workspace in Nexgensis OPS IQ
Analytics

AI Analytics

Quality Intelligence

Predictive signals, root cause suggestions and natural-language answers across your entire quality estate.

  • Predictive Quality
  • Root Cause Assist
  • NL Search
  • Executive Dashboards
Explore AI Analytics

Platform foundation

Every product inherits the same core.

Add a product and it inherits the same records, roles and validation evidence — no second integration project.

One Data Model

Records link across quality, lab and production.

One Security Model

Roles and permissions defined once, everywhere.

One Validation Package

Validation evidence shared by every product.

OPS IQ — One Platform for Every Quality Workflow

OPS IQ stands for Operations Process Suite with Integrated Quality — a unified architecture where quality, laboratory, manufacturing and asset data share one model, so intelligence and compliance work across the whole operation.

OPS IQCore

Enterprise Quality Management

Digitize quality processes with a unified eQMS that manages CAPA, deviations, audits, document control, change control, complaints, training, supplier quality, and risk management.

Products in this area

A validated path to go-live in 8–12 weeks

01

Discovery

Process mapping, gap analysis and success metrics agreed with your quality leadership.

02

Configuration

Your workflows, forms, roles and sites set up in your own tenant.

03

Validation

IQ/OQ/PQ execution using our pre-approved GAMP 5 package.

04

Training

Role-based enablement for QA, lab, production and IT super-users.

05

Go Live

Cutover with hypercare and parallel-run support on the floor.

06

Support

24×7 global support, quarterly releases and continuous improvement reviews.