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48-69 by 69 results
Implementation of the UDI according to EU-MDR – the medical...
Tuttlingen & Online, 78532 Tuttlingen
Conducting and evaluating a clinical trial
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Implementation of the EU MDR – EUDAMED
Tuttlingen & Online, 78532 Tuttlingen
Post-market surveillance and vigilance for medical devices
Tuttlingen & Online, 78532 Tuttlingen
Clinical evaluation and clinical testing of medical devices
Tuttlingen & Online, 78532 Tuttlingen
Cleaning validations within the manufacturing processes of m...
Tuttlingen & Online, 78532 Tuttlingen
Audits in the medical device industry (2 days)
Tuttlingen & Online, 78532 Tuttlingen
Practical reports: Pitfalls and liability risks in cross-bor...
Online
Cyber-secure software lifecycle processes for medical techno...
Online
Approval procedures in Great Britain and Switzerland
Tuttlingen & Online, 78532 Tuttlingen
Sustainably TOP in medical technology
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Biocompatibility and biological safety of medical devices
Tuttlingen & Online, 78532 Tuttlingen
The medical device consultant according to Section 83 MPEUAn...
Tuttlingen & Online, 78532 Tuttlingen
Tuttlingen & Online, 78532 Tuttlingen
Contractual structure of a clinical trial – legal agreements...
Online
Supplier management (purchasing control)
Tuttlingen & Online, 78532 Tuttlingen
Responsible person according to Art. 15 EU MDR – between res...
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