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03/03/1910
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IAS conducts IRCA Certified ISO 45001 Lead Auditor Training courses in association with EAS. IAS conducts courses world wide as open class room programme as per the pre-determined schedules, In-house programmes for exclusive for organizations, Online Virtual training.ISO 45001 LA course is a Tutor led course covers the planning, conducting, reporting of a third party 45001 audit. All activates are covered with more than 25 exercises. This mock audit programme gives a hands-on experience for the candidates in gaining knowledge and skills, thus provide a comprehensive approach in the learning process.
https://www.iascertification.com/iso-45001-2018-lead-auditor-training/IAS conducts IRCA Certified ISO 45001 Lead Auditor Training courses in association with EAS. IAS conducts courses world wide as open class room programme as per the pre-determined schedules, In-house programmes for exclusive for organizations, Online Virtual training.ISO 45001 LA course is a Tutor led course covers the planning, conducting, reporting of a third party 45001 audit. All activates are covered with more than 25 exercises. This mock audit programme gives a hands-on experience for the candidates in gaining knowledge and skills, thus provide a comprehensive approach in the learning process. https://www.iascertification.com/iso-45001-2018-lead-auditor-training/0 Comments 0 Shares 559 Views 0 Reviews -
ISO 13485 ist eine unabhängige Qualitätsmanagementsystemnorm für Medizinprodukte. Die Norm verlangt von einer Organisation, in einer oder mehreren Phasen des Lebenszyklus eines Medizinprodukts so zu implementieren, dass es die regulatorischen Compliance-Anforderungen für Medizinprodukte erfüllt. Die ISO 13485 Zertifizierung liefert den Nachweis, dass eine Organisation die Anforderungen an Medizinprodukte erfüllt, die dazu beitragen, dass sie während ihres gesamten Lebenszyklus frei von Kontaminationen, sterilisiert und sauber bleiben.
https://iasiso-europe.com/de/iso-13485-zertifizierung-in-deutschland/ISO 13485 ist eine unabhängige Qualitätsmanagementsystemnorm für Medizinprodukte. Die Norm verlangt von einer Organisation, in einer oder mehreren Phasen des Lebenszyklus eines Medizinprodukts so zu implementieren, dass es die regulatorischen Compliance-Anforderungen für Medizinprodukte erfüllt. Die ISO 13485 Zertifizierung liefert den Nachweis, dass eine Organisation die Anforderungen an Medizinprodukte erfüllt, die dazu beitragen, dass sie während ihres gesamten Lebenszyklus frei von Kontaminationen, sterilisiert und sauber bleiben. https://iasiso-europe.com/de/iso-13485-zertifizierung-in-deutschland/0 Comments 0 Shares 561 Views 0 Reviews -
The ISO 50001 Internal Auditor Training course teaches you how to perform an internal audit in accordance with the ISO 50001 standards for Energy Management Systems (EnMS). Delegates will be prepared to draft an audit report on the correct implementation and maintenance of a management system after completing this ISO 50001 training course. Delegates will also gain an understanding of auditing procedures in accordance with ISO 19011.
https://iasiso-europe.com/uk/iso-50001-internal-auditor-training-in-united-kingdom/The ISO 50001 Internal Auditor Training course teaches you how to perform an internal audit in accordance with the ISO 50001 standards for Energy Management Systems (EnMS). Delegates will be prepared to draft an audit report on the correct implementation and maintenance of a management system after completing this ISO 50001 training course. Delegates will also gain an understanding of auditing procedures in accordance with ISO 19011. https://iasiso-europe.com/uk/iso-50001-internal-auditor-training-in-united-kingdom/0 Comments 0 Shares 474 Views 0 Reviews
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