Handling of Certification Mark Misuse and Fraudulent Certificates for Product Certification

Document Reference: AC-QP-06
Version: 1.0 Effective Date: 15 December 2025 Prepared By: Prashant Vishwakarma Approved By: Anubhav Kumar Srivastava
For Reference Only: This document is provided for informational purposes.

1.0 Objective

The objective of this procedure is to define the process for monitoring, identifying, investigating, and addressing misuse of AQMA CERT certification marks and fraudulent certificates, including enforcement actions and record control.

2.0 Scope

This procedure applies to all AQMA CERT certification schemes and to any organization or individual using or referring to AQMA CERT certificates or certification marks. It covers all cases of unauthorized, incorrect, misleading, or fraudulent use of certificates or marks identified through internal activities, external complaints, market surveillance, or public information sources. The procedure applies to all AQMA CERT personnel involved in certification, surveillance, or market monitoring activities.

3.0 Responsibilities

3.1 Chief Executive Officer (CEO)

The CEO shall:

3.2 Head of Product Certification (HOD)

The HOD shall:

3.3 Operations Team

The Operations Team shall:

4.0 Operational Procedures

4.1 Control of the Use of Certificates and Certification Marks

4.1.1 AQMA CERT shall issue certificates and certification marks only for products that have successfully completed conformity assessment in accordance with the applicable certification scheme.

4.1.2 Certification applies only to the specific product model(s), batch(es), or sample(s) evaluated. Any other variants, additional models, or unrelated products are outside the certified scope.

4.1.3 For certification scheme type 1a, surveillance activities are not part of the certification cycle. Therefore, certification marks under this scheme shall not imply ongoing conformity beyond the evaluated sample and defined validity period.

4.1.4 For certification scheme type 3, continued use of the certification mark is subject to ongoing surveillance activities, such as audits, inspections, or testing, as defined in the applicable scheme.

4.1.5 AQMA CERT personnel attending exhibitions, trade shows, market visits, or industry events shall observe and verify compliance with certification mark usage rules and report any suspected misuse to the reporting manager or the HOD or QA without delay.

4.2 Misuse of Certificates or Certification Marks

4.2.1 Misuse includes, but is not limited to, the following situations:

4.2.2 Upon identification of any such misuse, the HOD shall formally issue a written notice to the certificate beneficiary that includes description of misuse, required corrective actions and a deadline for correction, with instructions of immediate discontinuation of misuse, including removal of marks, withdrawal of marketing material, and correction of public statements.

4.2.3 The Operations Team shall conduct a follow-up verification within provided deadline by HOD to confirm correction.

4.2.4 If misuse is not corrected or is repeated, the HOD shall recommend escalation to the CEO, which may include, but not limited to:

4.3 Handling of Fraudulent Certificates

4.3.1 Fraudulent certificates include:

4.3.2 Upon discovering or being informed of a suspected fraudulent certificate, the HOD and Operations Team shall immediately assess the case and collect evidence.

4.3.3 The HOD shall formally issue a written notice to the certificate beneficiary with instructions of immediate recall and discontinuation of use of the fraudulent certificate.

4.3.4 The notice shall clearly state that:

4.3.5 If the user of the fraudulent certificate ignores the warning or repeats the offence, the HOD shall recommend escalation to the CEO, which may include, but not limited to:

4.4 Record Keeping and Retention

4.4.1 Email correspondence and related electronic communications exchanged during identification, investigation, corrective action, and enforcement of certification mark misuse or fraudulent certificates shall constitute the official record for such cases. No separate case file or dedicated form is required.

4.4.2 Such records shall be retained and controlled in accordance with the Records Control (AC-QP-11).

5.0 Relevant Documents

6.0 Relevant Records

Amendment History
Version 1.0 - First Version – Initial Issue | Approved By: Anubhav Srivastava | Effective Date: 15 Dec 2025
Document Reference: AC-QP-06 | Version 1.0 | Effective: 15 December 2025