Always inspection-ready
Protocols, evidence and signatures live in a single system with an audit trail. No more rebuilding folders the week before an audit.
DiSQ · Digital Smart Qualification
Digital validation connected to your operation, not on its own island
DiSQ digitalises document management, SOPs, qualification protocols and CAPA deviations with traceability and electronic signature — and, unlike an isolated validation manager, it shares data with your warehouse, your production and your laboratory.
Validation and compliance across industry
PHARMALOGISTICSHOSPITALS
Benefits
What quality gains (and what it stops losing)
Deviations and CAPA under control
Every incident follows its workflow: logging, investigation, corrective action and a signed close-out. Nothing gets left in an email.
Knowledge doesn't walk out the door with people
SOPs and protocols, versioned, approved and accessible. New hires find 35 years of know-how, not a filing cabinet.
The question everyone asks
What does DiSQ mean?
DiSQ stands for Digital Smart Qualification: Labware's solution for taking qualification, validation and document management in regulated environments off paper and onto an intelligent digital system. "Smart" isn't decoration: protocols are generated from templates, evidence is captured at the point of work, and electronic signatures close every step with audit value.
And because DiSQ is part of the IP6 platform, validation doesn't live in isolation: it draws on the real data from your warehouse, your production and your laboratory.
Request a DiSQ demo →
The real screen, not a mock-up
Every protocol, with its approval status in plain sight
DiSQ's qualification tree organises clean rooms, cycles and protocols by customer, with each one's status — pending execution, released, approved — visible at a glance.
No exporting to a spreadsheet just to find out what's missing before the next audit.
Beyond documentation
DiSQ also manages this
AI assistant, your corporate brain
The core of your corporate knowledge: query SOPs, protocols and incident history in natural language, with no digging through folders.
Full project management
Create, run and coordinate internal and external projects with flexibility, cross-team collaboration and scalability, within the same system as validation.
Advanced risk management
Identify, assess and mitigate risks with an automatic traceability matrix that links every risk to its controls and evidence.
Differentiation
Why DiSQ instead of an isolated validation manager?
An isolated validation specialist doesn't manage your warehouse, your production or your lab.
Connected validation
- DiSQ shares data with WMS, LIMS and production: evidence is born where the work happens
- No exporting and importing between systems before every inspection
Compliance built in
- Electronic signature, versioning and audit trail on every document and protocol
- CAPA and deviation workflows with owners and deadlines
- Architecture compliant with GMP Annex 1 and FDA 21 CFR Part 11
One provider, the whole operation
- The same partner that's managed your warehouse and production since 1989
- Just another IP6 module: deployed with no monolithic project
For the technical profile
DiSQ functional detail
For quality and IT: what's underneath.
- Versioned documents with configurable review and approval workflows.
- SOPs with controlled distribution and read confirmation.
- Smart templates for generating qualification protocols.
- IQ/OQ/PQ protocols executable digitally, with evidence captured at the point of work.
- Electronic signature at every execution and approval step.
- Full traceability of requirements, tests and results.
- Offline mode available for environments without a constant connection, with sync afterwards.
- Logging and classification of incidents and deviations.
- CAPA workflows with investigation, actions, owners and effectiveness verification.
- Quality indicators and dashboards for management.
Frequently asked questions
Frequently asked questions about DiSQ
What does DiSQ mean?
DiSQ stands for Digital Smart Qualification: Labware's solution for moving qualification, validation and document management in regulated environments from paper to a digital system.
Protocols are generated from templates, evidence is captured right at the point of work, and electronic signatures close each step with audit value. Because it's part of the IP6 platform, it doesn't run in isolation — it draws on real data from your warehouse, your production and your lab.
How is DiSQ different from a standalone validation manager?
A standalone validation specialist doesn't manage your warehouse, your production or your lab. DiSQ does, because it's one more module of the IP6 platform:
- Shares data with WMS, LIMS and production: evidence is created where the work happens, with no export/import between systems before every inspection
- Electronic signature, versioning and audit trail on every document and protocol, by default
- A single provider for the whole operation, with the same expertise since 1989
Does DiSQ comply with GMP and FDA 21 CFR Part 11?
Yes. DiSQ's architecture is designed to comply with GMP Annex 1 and FDA 21 CFR Part 11, with electronic signature, document versioning and an audit trail at every execution and approval step.
What qualification protocols can DiSQ run (IQ/OQ/PQ)?
DiSQ runs IQ/OQ/PQ protocols digitally, capturing evidence right at the point of work with electronic signature at each step. It also keeps full traceability of requirements, tests and results, and offers offline mode for environments without constant connectivity, with later synchronization.
How does DiSQ handle deviations and CAPA?
Every incident follows its own flow in DiSQ: logging, investigation, corrective action and signed closure — nothing is left hanging in an email.
- Logging and classification of incidents and deviations
- CAPA workflows with investigation, actions, owners and effectiveness verification
- Quality indicators and dashboards for management
What is the DiSQ AI assistant?
It's the core of your corporate knowledge inside DiSQ: it lets you query SOPs, protocols and incident history in natural language, instead of digging through folders and versions by hand.
Does DiSQ manage projects and risks too, or just documentation?
It goes beyond document management:
- Full management of internal and external projects, with team collaboration inside the same system as validation
- Advanced risk management, with an automatic traceability matrix linking each risk to its controls and evidence
Is the knowledge documented in DiSQ lost if an employee leaves?
No. SOPs and protocols stay versioned, approved and accessible within the system. New hires find the organization's accumulated know-how, not a paper filing cabinet that depends on one person.
IP6 platform
Other IP6 solutions that complete your industrial digitalisation
Warehouse management
WMS with real-time traceability: inventory reliability above 99%, native batches, expiry dates and quarantines.
Learn more →Quality & lab control
Paperless test recording and validation, with batch release connected to warehouse and production.
Learn more →Paperless production
Guides the operator step by step through every production stage, to avoid errors and achieve the highest quality for the production batch.
Learn more →Weighing & dispensing booth
Guided weighing with connected scales: zero dosing errors and every gram documented.
Learn more →Want to dive deeper into the regulation? Read the GMP Traceability guide →
Next step
See DiSQ with a real protocol on screen
A 30-minute demo: from template to signed protocol, with real evidence.
No commitment