Services

  • ISO 22301 Business continuity management system with Kiwa: Prepare for disaster, disaster, and accident-related business disruptions.
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  • NEN 7510 Information Security certification with Kiwa: secure your medical information, build trust in your brand.
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  • ISO 37001 Anti-bribery Management Systems Certification with Kiwa: prevent, detect and address bribery to build trust in your brand and boost your business.
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  • ISO 13485 Medical Devices Certification with Kiwa: ensure quality, build trust and comply with regulations in the medical devices sector.
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  • ISO 14001 Environmental Management Certification with Kiwa: reduce waste, gain customer trust and be competitive.
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  • Kiwa boasts a wide and in-depth experience as Notified Body from over 20 years in Medical Devices certification, with thousands of products already certified, providing all the necessary services to get complete answers and reliable information on medical devices certification services according to 93/42/EEC Directive.
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  • Kiwa offers to Organizations the opportunity to carry out electrical safety, electromagnetic compatibility and any functional test in its laboratories, with respect to the harmonized Standards.
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  • OHSAS 18001 certification with Kiwa: reduce accidents, improve conditions and attract talent.
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  • ISO 10002 customer satisfaction certificate with Kiwa: Increase your performance, meet the needs of your customers and increase your profits.
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  • ISO 9001 Quality Management Systems Certification with Kiwa: improve your performance, meet customers’ needs and increase your profit.
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  • Kiwa Blackwood | Electrical Safety Compliance
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  • GMP Medical Devices Certification with Kiwa: prove the quality of your medical devices, open up new markets and meet customers’ needs.
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  • In order to be freely traded on the European Union and EFTA market, the products have to be conform to the pertaining product directives and have to be CE marked. For what concerns the CE mark for Medical Devices, the Directive 93/42/EEC is applied, that has been successively integrated by European directives
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  • Following the adoption of the legislative resolution of the European Parliament, who approved in the first days of April the position of the European Council regarding the Medical Devices Regulation (MDR) introduction, the Medical Devices Regulation was published on the Official Journal on 5 May 2017.
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  • EMAS certification with Kiwa: reduce your environmental impacts, engage employees and boost your reputation.
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  • VCA, VCO and VCU health, safety and environment certification with Kiwa: create safe working conditions for contractors and reduce accidents.
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  • Especially in construction sector sustainability efforts are increasing. This requires companies to identify and declare the environmental impact of their products. The Environmental Product Declaration is used as an effective tool for this purpose.
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  • As Kiwa  Turkey, we have prepared a series of training programs for the continuous improvement of effective performance management systems and practice to find out the full impact of the ISO 27001 everyone from beginners to professionals. In ...
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  • WPQR is the process of examining the welding procedure during the compliance process according to the relevant standards (manufacturer's production, supervising the welding test, carrying out the testing procedures and evaluating them).
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  • Kiwa | MDR Medical Devices Regulation Training
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