Quality management: sampling, inspection and release – the same procedure every time
Whether incoming goods, ongoing production or final inspection: taking samples, testing, assessing and releasing always follows the same principle – with many people involved and fixed deadlines. CaRD Plan keeps these procedures as templates, hands the steps to the people responsible and proves at the end who checked what and when.
Request a demoRecurring inspection procedures as templates
Every inspection procedure is set up once as a template – with steps, sequence, owners and expected times. For every batch, every sampling round or every audit a plan of its own is created from it that runs exactly like last time.
- Incoming goods inspection, in-process sampling, final inspection and release
- Product tests and stability tests with fixed test points
- Internal audits and supplier audits with preparation, execution and actions
- Complaints and corrective actions – every step with an owner and a date
Result and finding right on the test step
Whoever tests reports back on the step – at the workstation or by phone on the line: done, with a reading or finding as a comment, optionally with a photo or test report attached. Following steps are released only when their predecessors are done – so the release never comes before the test.
Four-eyes principle and releases
Second check and release are steps of their own, assigned to another person. Anyone who forces a step anyway has to give a reason – it is stored in the history with person and time. Roles and access grants define who may read, report back or plan.
Complements your QMS
CaRD Plan replaces neither LIMS nor CAQ software nor your quality manual: test instructions, characteristics and limits stay there. CaRD Plan steers the execution by many people and delivers the closing report and archive as evidence – plus lead times that show where a procedure gets stuck.

Frequently asked questions
Does CaRD Plan replace our LIMS or CAQ software?
No. Sample and measurement data management, test characteristics and statistical analysis stay in your systems. CaRD Plan steers the procedure of the people involved and proves who completed which step when; readings and findings are recorded as a comment or attachment on the step.
How does a recurring sampling round work?
The sampling procedure is a template. For every round a plan is created from it in a few clicks; the people responsible see their steps under “My tasks” – also on the phone – and report back. The overview shows what is open, in progress or delayed.
Is CaRD Plan suitable for audits?
Yes, for the procedure: preparation, execution, report and actions become steps with owners and dates. Observations are recorded as findings on the step; the actions are tracked as a plan of their own until they are done.
More use cases
Management of Change
Implement product and process changes in a structured way: steps, owners and approvals in one plan, every step recorded with person and time.
Learn more →Product development process
Product development from idea to production release: phases and quality gates as a template, tasks per department, live feedback and evidence for every gate.
Learn more →ERP cutover planning
ERP go-live without spreadsheet chaos: cutover plan as a template, rehearsals, live board and closing report – for SAP S/4HANA, Dynamics 365 or JD Edwards.
Learn more →Acceptance and test plans
Factory and site acceptance, software tests and validation runs as a plan: test steps in a fixed order, findings on the step, the protocol as PDF.
Learn more →Maintenance plans and shutdowns
Maintenance, shutdowns and overhauls of complex products and plants: the procedure as a template, teams live, every step recorded with person and time.
Learn more →System replacement and harmonisation
Move sites and companies onto one system, one after another: the procedure as a template, every wave its own plan, findings carried into the next one.
Learn more →Machinery and plant engineering
Commissioning, test sequences and acceptance at the customer as a plan: test steps in a fixed order, readings as findings, report-back straight from the phone.
Learn more →Medical devices, pharma and laboratory
For FDA-regulated and other regulated manufacturers: qualification, validation runs and changes as a plan, every step with person, time and comment.
Learn more →Aviation, energy, transport
Retrofits, product changes and system changeovers in safety-critical industries: exact order, Force only with a reason, complete history.
Learn more →Food and beverage
Product changeovers with allergen cleaning, HACCP checks, traceability tests and audit preparation as a plan – every step evidenced with person and time.
Learn more →See your own procedure in CaRD Plan
Tell us briefly what it is about – in 30 minutes we show you what the plan looks like.
CaRD Gesellschaft für EDV-Beratung mbH
Gutenbergring 2 · 69168 Wiesloch, Germany
Phone +49 6222 9256-0 · E-mail info@card.de