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Vişne Chem

Management System

Integrated Management System

Quality, environment, occupational health and safety, energy and information security are run as one system. VisneChem products are made under that system, certified to five ISO standards and covered by the CE conformity certificate held by Vişne Madencilik.

Why one system rather than five separate ones

An integrated management system means running five separate management standards under one set of procedures, one document structure, one internal audit programme and one management review. Quality, environment, occupational health and safety, energy and information security all share ISO's Harmonized Structure (Annex SL): context of the organisation, leadership, planning, support, operation, performance evaluation and improvement arrive in the same order under the same clause numbers. Because Vişne Madencilik, the group behind VisneChem, gathers that shared skeleton into a single system, the quality record and the environmental record of a process are not kept in two ledgers but in one.

What that means in practice shows up on the kiln line. The fuel feed of a lime kiln falls under four standards at once: calcination temperature governs product reactivity and therefore belongs to ISO 9001, stack emissions to ISO 14001, thermal consumption per tonne to ISO 50001, and hot-surface and dust exposure to ISO 45001. Under separate systems the same kiln is examined four times, by four teams, against four sets of measurements, and the resulting decisions cut across each other — trimming fuel to meet an energy target can pull down the available CaO and the reactivity of the product. At the Çelemli and Narlı factories, where the kilns are, the kiln line is managed by a single process owner, within a frame where all four measures are read from the same table.

The system does not stop at the office door; it covers the chain from the quarry face to the weighbridge. Limestone purity at the crushing-and-screening stage, available CaO at the kiln outlet, particle size distribution after grinding and the traceability record of every batch leaving the silo all hang on the same chain. Our entire product range — from quicklime to ground calcium carbonate — is the output of that chain; when a customer report comes in, what is traced backwards is not the product itself but the process parameters that batch passed through.

The second gain of a single system shows in the audit load. Had the internal audits of five standards been planned separately, a plant would carry five audit programmes, five corrective action lists and five management review meetings a year. In an integrated programme the same process is audited once but from five angles; findings fall into one corrective action pool, root cause analysis is done once, and closure is tracked by the same committee.

The standards that make up the system

The six certificates below document different faces of the same management system: five are ISO management system standards, the sixth is a conformity certificate covering the placing of product on the European market. The Version column gives the year of the standard edition the certificate rests on; CE has no such edition year, conformity being assessed against the legislation of the market where the product is placed.

StandardScopeVersion
ISO 9001Quality management system — process control, product conformity, batch traceability and handling of customer reports2015
ISO 14001Environmental management system — identifying and controlling emission, waste, water and land impacts2015
ISO 45001Occupational health and safety management system — hazard identification, risk assessment, prevention of accidents and occupational disease2018
ISO 50001Energy management system — measuring, monitoring and reducing thermal and electrical consumption per tonne2018
ISO 27001Information security management system — confidentiality, integrity and availability of information, and business continuity2022
CEEuropean Conformity certificate — declaration of conformity for placing the product on the European market

Twelve commitments

The policy consists of twelve written commitments. They are not a statement of intent but clauses for which records are sought at internal audit: under each commitment sits an indicator that measures it, a record that produces that indicator, and an owner who reviews the record. Everything from production decisions to technical services maps onto a record filed under the relevant commitment.

  • Customer Satisfaction

    We commit to ensuring the continuity of customer satisfaction at all levels of our operations.

  • Performance & Efficiency

    We commit to improving company performance and production efficiency through innovative practices.

  • Quality Production

    We commit to providing high-quality production and services in all activities we carry out.

  • Legal Compliance

    We commit to complying with applicable legal regulations and fulfilling all regulatory requirements.

  • Environmental Responsibility

    We commit to reducing, controlling and preventing negative environmental impacts resulting from our activities.

  • Waste Management

    We commit to ensuring recycling of wastes and proper disposal of non-recyclable wastes.

  • Occupational Health & Safety

    We commit to developing systems to ensure occupational health and safety and prevent workplace accidents.

  • Continuous Improvement

    We commit to continuous improvement in Health – Safety – Environment.

  • Information Security

    We commit to ensuring information security and business continuity in our activities.

  • Technology Adoption

    We commit to following and implementing technological developments and continuing R&D investments.

  • Employee Development

    We commit to supporting the development of our employees and adopting a participatory management approach.

  • Participatory Management

    We commit to continuously improving our Integrated Management System performance with the participation of our employees.

We commit to continuously improving our Integrated Management System performance with the participation of our employees.
Vişne Madencilik Üretim Sanayi ve Ticaret A.Ş. — Integrated Management System Policy

Independent auditing and the validity of certificates

To build sustainable success and trust, all our processes are regularly evaluated by independent audit organisations. Certification does not rest on the organisation's own declaration but on an on-site audit by an accredited certification body: the auditor looks not for the written procedure but for the record showing the procedure was followed — the shift log, the calibration label, the training attendance sheet, the closure date of a corrective action. Images of the valid certificates are published per facility on the certificates page.

Management system certification runs on a three-year cycle: the initial certification audit is followed by surveillance audits in the intervening years and a recertification audit at the end of the third year. A certificate is therefore not a one-off approval but a condition whose continuity is proven by audit; a major nonconformity raised at surveillance can suspend the certificate if it is not closed. Product conformity runs on a separate axis: in fields such as construction and building materials, placing a product on the market depends not on the management system certificate but on the harmonised standard applicable to that product and on the declared performance. The two do not substitute for each other; a customer file usually asks for both.

Certificates are issued per facility; those held separately for Çelemli, Narlı and Gündoğan Maden show how one system is applied at three different production points. If a current copy is needed for a tender file, a customer audit or a supplier approval process, it can be requested through contact; stating which facility's certificate and which standard's scope is required lets the reply come back in a single step.

Sample and dose recommendation for this process

Describe your current usage and target; our technical team will come back with a suitable specification and a starting dose.