The Quickflow platform · No-code for GxP
One platform,
many GxP applications.
Describe what the lab needs in a sentence. Quickflow builds it, tests it, writes the validation file from URS to release notes, and waits for your scientists and QA to sign. Nine applications already run this way.
Step 1 of 7. You describe the application in plain language.
Describe the application
AI understood
- Column register form
- Life and expiry rules
- QA approval workflow
- Usage dashboard
- Monthly usage report
- Audit trail
One description becomes forms, rules, an approval workflow, an analytical dashboard, a report and an audit trail. Click a stage to jump, or let it run.
Validated from day one
Quickflow checks the boxes a regulated organisation has to check before anything else, in every application it builds.
21 CFR Part 11 and EU Annex 11
Audit trail, e-signatures and unique users in every application, not as an add-on.
CSA by design
Risk-scaled validation documents produced as the app is built, aligned with GAMP 5.
Access and identity
Role-based permissions, single sign-on with Active Directory, controlled privileges.
Integrations
LIMS, CDS such as Empower and Chromeleon, SAP, instruments over RS232 and Ethernet.
Hosting in your region
On AWS, in Mumbai by default or the region your data-residency rules require, with the same validated package in every environment.
AI with governance
The AI drafts, tests and documents. Nothing is released without a human signature.
Six steps. Two are yours.
You describe and you approve. The AI builds, tests, documents and, once you sign, promotes.
Step 1 · You
Describe
In plain language, or hand over a URS.
Step 2 · AI
AI builds
Forms, rules, workflow, dashboards and reports.
Step 3 · AI
AI tests
End to end, with screen evidence for every case.
Step 4 · AI
AI documents
The CSV/CSA file, URS to release notes.
Step 5 · You
You review and approve
Every artefact, e-signed by a named person.
Step 6 · AI
VMS promotes
Dev to QA to Prod, only on approval.
AI testing
Tested end to end with evidence
Every form, rule, signature and role is exercised before a person looks at it. Each case leaves a screen as evidence.
Column register app · v2.0 · End-to-end test run
RunningTest cases
0/140
Passed
0
Evidence captured
0 screens
- Forms and field validationqueued
- Rules and calculationsqueued
- Workflow and e-signaturesqueued
- Roles and accessqueued
- Audit trailqueued
- Reports and dashboardsqueued
AI documentation
URS to release notes, as it is built
The validation file is written alongside the app, risk-scaled the CSA way. Your CSV team reviews and signs each document.
- URSUser requirement specificationdrafted from your description and the generated app
- RARisk assessment (CSA)drafted from intended use and patient/product risk
- FS · DSFunctional and design specificationdrafted from the forms, rules and workflow as built
- IQ · OQ · PQQualification protocols and scriptsdrafted from the requirements, risk-scaled
- TRTest evidence and summary reportdrafted from the AI test run
- RTMRequirements traceability matrixdrafted from URS ↔ FS ↔ tests
- RNRelease notesdrafted from the approved version in VMS
Version Management System
Development to Quality to Production, on approval only
AI builds and tests
- Same app, same configuration
- Nothing edited by hand
UAT and QA review
- Same app, same configuration
- Nothing edited by hand
Live, validated
- Same app, same configuration
- Rollback in one approval
Built for life sciences, in numbers
- 10
- Ready applications
- 7
- CSV/CSA documents per app
- 3
- Environments
- 2012
- Serving life sciences since
Method validation to user access management
URS to release notes, AI drafted
Dev, Quality, Production
Team behind Webosphere
AI Digital Scientists
The same platform runs the Digital Scientist
Quickflow MVS is an application built this way: forms for protocols and worksheets, rules for ICH Q2(R2) criteria, a workflow with three human signatures, dashboards for validation status, reports for submission and an audit trail throughout. The Digital Scientist is what the platform becomes when it is given a scientist's job.
Why it is different
Generic platforms leave compliance, testing, documentation and promotion to you. Quickflow does them inside the platform.
| Capability | Generic low-code | Custom development | Quickflow |
|---|---|---|---|
| 21 CFR Part 11 audit trail and e-signatures in every app | ~ | ~ | |
| AI builds forms, rules, workflow, dashboards, reports | ~ | ||
| AI end-to-end testing with evidence and report | |||
| AI-generated CSV/CSA documentation, URS to release notes | |||
| Controlled Dev → QA → Prod promotion with approval gates | ~ | ~ | |
| Ready life-science applications, MVS to UAM | |||
| Digital Scientists that own the evidence |
~ means possible with extra configuration, validation effort or third-party tools.
10 applications already built
Start from one of these, or describe your own. See all applications
- Drafts the ICH Q2(R2) protocol from the MOA
- Pre-fills worksheets and captures instrument data
- Compiles an audit-ready report with full traceability
- Your scientist reviews and e-signs every step
Laboratory
- eSheet · Calculation sheetsTurns laboratory calculations into secure web-based forms with access control and fine-grained permissions. Every change is versioned and audit-trailed.
- ELN · Electronic Lab NotebookReplaces paper notebooks with structured, compliant digital records that improve collaboration and searchability.
- eLogbook · Electronic LogbookDigitises traditional logbooks for equipment usage, calibration and similar activities with secure electronic records.
Quality
- eQMS · Quality Management SystemManages change controls, deviations, CAPA, market complaints and OOS investigations with the precision inspectors expect.
- eDMS · Document Management SystemControls SOPs, STPs, protocols and other GxP documents with audit trails, version control and structured approval.
- Alarm Trending · Alarm Trending ManagementReads alarms live from instruments and building systems, groups them into events and explains the cause, so drift is caught before it becomes a deviation.
- CPV · Continued Process VerificationCollects, analyses, trends and reports process data in real time to confirm processes stay within predefined quality criteria.
IT and access
- UAM · User Access ManagementEmployee details come from HRMS, or are entered in UAM, and the requestor picks the systems. After manager review and system owner approval, Quickflow Vision grants or removes access on each selected system, with 21 CFR Part 11 audit trails.
- ECS · Endpoint Control SystemKeeps Scientific Rawdata on GxP workstations original and complete: cut, copy, paste, rename, delete and drag-and-drop are removed from protected folders, and every computer confirms live that its approved controls are in force.
See what Quickflow can build for you.
Bring one process that lives in spreadsheets or paper today. We will build it with you in a working session, run the AI test suite and show the documentation it produces.
Before
Bring one process from paper or Excel
Working session
We build it with you, live
Same session
The AI tests it end to end
Then
You see the documentation it produces
The platform
Questions about the platform
What IT, CSV and quality teams ask before they build their first application.
Pharmaceutical and life-science organisations that need applications in GxP environments: QC and AR&D laboratories, quality assurance, manufacturing and the IT and CSV teams that validate systems for them.
Any process that today lives in paper, Word or Excel: registers, logbooks, calculation sheets, investigations, reviews, requests and approvals. Every app has forms, rules, workflow, dashboards, reports and an audit trail. Nine ready applications, from method validation to user access management, were built the same way.
The AI builds, tests and documents. It never approves. Every artefact it produces, from a form to a release note, is reviewed and e-signed by a named person, and the whole history is in the audit trail.
As it is built. The platform generates the URS, risk assessment, functional and design specifications, qualification scripts, test evidence, traceability matrix and release notes, scaled to risk the CSA way. Your CSV team reviews and approves them.
The Version Management System packages the approved version and promotes it from Development to Quality to Production through approval gates. Nobody copies configuration by hand, and rollback is one approval.
Generic platforms leave compliance, testing, documentation and promotion to you. Quickflow does them inside the platform, for life sciences specifically, and ships with ready GxP applications and Digital Scientists.