Bureau Veritas

Since 1828, Bureau Veritas has been a part of the maritime and offshore industry. A few years later, more than 10,000 ships were registered in our ship register, and we had established offices in all major ports in the world. Today we are one of the largest global actors with offices in 140 countries, where we offer a wide range of services.

We offer: Classification and inspection of ships, approval of maritime and offshore equipment, Design review and plan approval services, oil and gas services and training courses.

We help ship owners, shipbuilders, shipyards, equipment manufacturers, insurance companies, brokers and flag states to ensure compliance with the international rules and regulations regarding quality, safety, environment and work environment.


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MDR and ISO 13485 for distributors, importers (english) - online

We provide online course about MDR and ISO 13485 for distributors, importers and authorized representatives in english. MDR sets clear requirements for distributors, importers and authorized representatives, and the regulation describes the requirements from the manufacturer to the supplier.

Sted Dato Varighet Pris
Nettkurs / nettstudie Nettkurs / nettstudie 1 day 5.000 kr  

MDR and ISO 13485 for subcontractors (english) - online

We provide online course about MDR and ISO 13485 for subcontractors in english. The MDR requirements for manufacturers have increased, and manufacturers have to take responsibility for controlling their subcontractors.

Sted Dato Varighet Pris
Nettkurs / nettstudie Nettkurs / nettstudie 1 day 5.000 kr  

MDR, ISO 13485 and quality management system (english) - online

We provide online course about MDR, ISO 13485 and quality management system requirements in english. The Medical Device Regulation (MDR) set requirements for the manufacturer´s quality management system (QMS) as well as for the products.

Sted Dato Varighet Pris
Nettkurs / nettstudie Nettkurs / nettstudie 1 day 5.000 kr  

MDR, ISO 13485 and the post marketing feedback (english) - online

We provide online course about MDR, ISO 13485 and the post marketing feedback Requirements in english. MDR requirements for the technical documentation have been tightened up. The technical documentation is a prerequisite for the CE marking of medical devices.

Sted Dato Varighet Pris
Nettkurs / nettstudie Nettkurs / nettstudie 1 day 5.000 kr  

MDR, ISO 13485 and the technical documentation (english) - online

We provide online course about MDR, ISO 13485 and the technical documentation in english. The classification of medical devices has been changed to a higher class for some medical devices. It places new demands on manufacturers and their product documentation.

Sted Dato Varighet Pris
Nettkurs / nettstudie Nettkurs / nettstudie 1 day 5.000 kr  

OHSMS ISO 45001:2018 Lead Auditor Arbejdsmiljø (CQI and IRCA)

Vi tilbyder kursus om OHSMS ISO 45001:2018 Lead Auditor Arbejdsmiljø (CQI and IRCA-certificeret). Kurset udbydes af: Bureau Veritas Certification Denmark A/S. Undervisningens varighed: 5 dage.

Sted Dato Varighet Pris
Danmark, Severin Kursu... Danmark 5 dager 25.500 kr  
Danmark, Sinatur Hotel... Danmark 5 dager 25.500 kr  

OHSMS ISO 45001:2018 Lead Auditor Arbejdsmiljøkursus

Vi tilbyder OHSMS ISO 45001:2018 Lead Auditor Arbejdsmiljøkursus. Ved gennemførelse vil du være i stand til at planlægge gennemføre og afrapportere effektive 1, 2 og 3 parts audits af arbejdsmiljøledelsessystemer i henhold ISO 45001:2018 og i overensstemmelse med ISO 19011 og ISO 17021 standarderne.

Sted Dato Varighet Pris
Danmark, Severin Kursu... Danmark 5 dager 25.500 kr  
Danmark, Sinatur Hotel... Danmark 5 dager 25.500 kr  

Opbygning af HACCP-systemer

På kurset i opbygning af HACCP-systemer får du - med udgangspunkt i en konkret proces - en grundig introduktion til de 12 HACCP-trin og 7 HACCP-principper samt forskellige værktøjer, du med fordel kan anvende til udarbejdelse af din virksomheds HACCP-system.

Sted Dato Varighet Pris
Danmark Danmark 2 dager 12.500 kr  
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