← Knowledge base
KNOWLEDGE BASE / AUDITS AND ACCREDITATION

What actually happens during certification?

An audit is one stage, not the entire process

This category explains the roles of the auditor, technical reviewer and decision-maker, accreditation principles, impartiality, audit preparation and practical management of nonconformities.

Questions we clarify
Who can carry out a RecyClass audit?
Does the auditor issue the certificate?
What is a technical review?
How does accreditation differ from scheme recognition?
How should evidence be prepared and a nonconformity closed?
CERTIFICATION PROCESS

From enquiry to decision

01
Scope and preparation
Scheme, site, products, modules, documentation and data.
02
Audit
Assessment of documents, processes, data and evidence.
03
Nonconformities and actions
Cause analysis, corrections, corrective actions and evidence.
04
Review and decision
Independent stages where required by the relevant scheme.
ESSENTIAL ARTICLES

Preparing for an audit, the audit itself and its outcome

AUDITOR, TECHNICAL REVIEW AND DECISION

Separate roles strengthen the process's credibility

Auditor
Collects evidence, assesses conformity and documents findings.
Technical review
Independently examines the process documentation where required by the scheme.
Certification decision
The authorised person makes the decision under the applicable rules.
Impartiality
The outcome must follow the evidence, not the business relationship.
ACCREDITATION

Accreditation covers a defined scope, not a body's entire service offering

When assessing a process's status, check the current accreditation scope and the specific scheme. Recognition by a scheme owner and accreditation are separate mechanisms.

Almaland: PCA AC 246
Recycling Process and Recycled Plastics Traceability are delivered within the relevant accredited scope; Sorting Process and RecyClass Recyclability operate under RecyClass recognition outside the scope of PCA AC 246.

WHAT DETERMINES AUDIT QUALITY

A finding needs evidence and a decision needs a clear basis

An audit is not a search for individual documents. Its purpose is to check whether the system described by the organisation works in practice and whether appropriate evidence demonstrates this.

SCOPE

Before the audit, clearly define the scheme, sites, processes, products, materials and additional modules. The right scope is essential to assessing the right evidence.

AUDIT EVIDENCE

Evidence can include a document, production record, invoice, weighing record, certificate, laboratory report, system record, process observation or verified information from an interview.

SAMPLING

An audit does not involve checking every document from the entire year. Representative samples are selected, but the organisation must demonstrate that the system works throughout the certification scope.

NONCONFORMITY

A nonconformity should identify a requirement, evidence and a specific gap. It is neither a penalty nor a general opinion about the organisation.

CORRECTIVE ACTION

Addressing the immediate effect alone may be insufficient. Depending on the case, cause analysis, action to prevent recurrence and evidence of effective implementation may be needed.

REVIEW AND DECISION

Where the relevant scheme requires it, the audit is followed by separate technical review and certification decision stages. Finishing the audit visit is not the same as issuing a certificate.

RELATED AREAS

Credibility depends on competence and independence

The audit is only one part of the overall system. Also check the body's formal status, staff competence and impartiality arrangements.

AUDITS AND ACCREDITATION

Want to prepare your organisation for an independent assessment?

Start with the right scope, source data and evidence that genuinely reflects the process.