Your approved supplier list is only as good as the day you last checked it.
Clover helps manufacturers qualify suppliers, keep quality certifications current, and run corrective actions to verified closure, so supplier quality is a system, not a spreadsheet someone maintains.
| Company | Assigned to | Completion |
|---|---|---|
|
Northfield Precision Castings
|
General Management
|
0%
|
|
Ridgeline Polymers
|
Marcus Johnson
|
40%
|
|
Calder Fastener Co.
|
Aria Turner
|
50%
|
Built for manufacturers running supplier quality on spreadsheets.
You have an approved supplier list, a quality manual that says how suppliers get qualified, and an audit finding that says the two don't match. The certifications live in a shared drive, the SCARs live in email, and the person who knows which suppliers are actually in good standing is one resignation away from taking that knowledge with them.
Clover turns the supplier quality program you already wrote into workflows that actually run. We work with OEMs and contract manufacturers who need it live in weeks, not months.
Where supplier quality breaks down
Qualification is a checklist that lives in someone's head.
Your quality manual defines what an approved supplier must provide: certifications, quality agreements, process documentation. In practice, qualification is emails and a spreadsheet column that says 'approved' with no record of what was actually checked, by whom, or against what standard.
Certifications expire quietly. Auditors find them loudly.
ISO certificates, quality system registrations, and material certs were current when collected. Whether they're current now depends on whether anyone looked recently. The gap surfaces at the worst moment: a customer audit, a nonconformance investigation, a recall inquiry.
Corrective actions close because everyone stopped talking about them.
You issue a SCAR, the supplier replies 'contained and corrected,' and the thread dies. No root cause on record, no verification, no way to see that this is the same supplier's third labeling nonconformance this year. Your CAPA discipline is only as strong as your inbox archaeology.
Qualification, certifications, and corrective actions, on one system.
Clover is a supplier operations platform for manufacturers. It structures the work between you and your supply base (qualification, certification upkeep, corrective actions, document collection) and leaves behind the quality record your auditors and customers expect.
Supplier qualification that runs your actual criteria
Define what qualifying a supplier requires by category: certifications, quality agreements, process documents, assessments. Suppliers complete it through guided tasks, AI validates documents at submission, and the approval decision lands on the record with who made it and why.
Quality certifications that stay current
Every time-bound certification carries its expiry date. Renewal tasks fire automatically ahead of lapse, replacements are validated against your requirements at upload, and every version is retained, so the approved supplier list reflects today, not qualification day.
Corrective actions to verified closure
A SCAR in Clover is a structured workflow: the nonconformance documented, the supplier's root cause and corrective plan required before the task can advance, evidence attached, and closure only on your verification. The whole loop stays on the supplier's record.
Supplier quality data is exactly what AI is good at. If the data exists.
Manufacturing teams are piloting AI for supplier risk scoring, nonconformance pattern detection, and audit preparation. The bottleneck isn't the AI. It's the data. SCARs scattered across inboxes and certifications in a shared drive give an AI nothing to reason over.
Clover's data is different. Every corrective action carries its root cause, resolution, and verification. Every certification carries its validity history. When you ask 'which suppliers have repeat nonconformances with root causes that didn't hold?', Clover's data can answer that. Your inbox can't.
Explore the workflows behind this solution
Supplier Assessment
Qualify suppliers against your criteria before they're approved: guided questionnaires, validated documents, a scored decision on record.
Learn moreCorrective Actions
SCARs and CAPAs as structured workflows: root cause required, evidence attached, closure verified, the full loop on the supplier record.
Learn moreCertificates & Renewals
ISO certificates, quality registrations, and insurance tracked to expiry, with renewal drives that run themselves and full version history.
Learn moreSupplier Onboarding
Quality agreements, certifications, and process documentation collected before the first PO, in one structured workflow.
Learn moreSupplier Record Management
Every qualification decision, certification, and corrective action on one supplier record, so supplier reviews and scorecards run on evidence, not spreadsheets someone assembles.
Learn moreCompliance Campaigns
PFAS, conflict minerals, and ESG data requests sent across your supply base, with every response validated and tracked to completion.
Learn moreFrequently asked questions
You define what qualifying a supplier requires by category: certifications, quality agreements, process documentation, assessment questionnaires. Suppliers complete the requirements through guided tasks, AI validates documents at submission, and the qualification decision is recorded with who approved it, against what criteria, and any conditions attached. Requalification runs the same way, on your cadence.
Yes. Every time-bound certification (ISO 9001, industry-specific registrations, insurance, material certs) carries its expiry date in Clover. Renewal tasks fire automatically ahead of lapse, replacements are validated against your requirements at upload, and every version is retained, so you can show continuous certification for any supplier on any date.
A corrective action in Clover is a structured workflow: the nonconformance documented with evidence, the supplier's response walked through required steps (root cause analysis, corrective plan, proof of implementation), and closure only on your verification. The complete loop stays on the supplier's record, so repeat issues are visible as repeats, not treated as new.
Yes. Clover keeps every qualification decision, certification lapse, corrective action, and resolution on the supplier record as the work happens. That history is the raw material for supplier reviews and scorecard conversations: how many issues, how quickly they closed, whether fixes held. You configure the views your review process needs rather than assembling data by hand.
Yes. The platform is configured to your requirements, not hardcoded to a position in the supply chain. Contract manufacturers use it to manage their material and component suppliers; OEMs use it across their supply base; some teams are both, running customer-facing compliance on one side and supplier-facing programs on the other.
Weeks, not months. Clover is configured, not custom-coded: your qualification criteria, certification requirements, and corrective action steps are set up as workflows on the existing platform. Most teams start with the process that hurts most, prove it, and expand from there.
A SCAR is a formal request from a manufacturer asking a supplier to investigate a nonconformance, find the root cause, and put a fix in place. A complete SCAR covers containment, root cause analysis, the corrective and preventive actions taken, and evidence that the fix works. The manufacturer verifies that evidence before the SCAR is closed.
See Clover built around your supplier quality program
We'll walk through your qualification and corrective action process in a live product walkthrough, and show you what a complete supplier quality record looks like in practice.
We start with your problems, then show you how Clover would solve them. A real walkthrough with someone who knows supplier quality.
Typical deployments cost less than a single supplier quality engineer.
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