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Leventon

As a manufacturer of Medical Devices, Leventon has a Quality Policy that is aimed at fully meeting the expectations of customers (distributors and, through them, hospitals centers, health personnel and patients) as regards the Quality and Service of its products, as well as all legal and regulatory requirements of the sector.

Highest quality assurance standards:
CE Mark , Leventon FDA Registered establishment since 1985, MDSAP Certification – Medical Device Single Audit Program (April 2021), ISO 13485:2016,  MDR – EU Medical Device Regulations (2021)

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EAHP Forum

All the EAHP team is working on providing a Forum that can help connect all the members in Conversations and Groups to talk about important matters for the European Hospital Pharmacist.

The Forum will be accessible for all the EAHP members, you don’t have to create a new account to browse and participate.

Conversations and groups

The Conversations will be moderated by our team to provide documents and relevant topics for the community.

The Groups will connect all members that share a category. Members who work on the same assocation, on the same hospital, that have the same role, etc.

Stay tuned for the realase of the forum. Soon on EAHP.