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16 - 20 June 2025

MOA BerlinBerlin, Germany

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16 - 20 June 2025

MOA BerlinBerlin, Germany

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Day One – 10 June 2024
Day Two – 11 June 2024
Day Three – 12 June 2024
Day Four – 13 June 2024
Day Five – 14 June 2024

Jun 12

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Day Three – 12 June 2024Wednesday, 12 June 2024 - CEST (Cent Europe Summer, GMT+2)

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Biocompatibility Workshop: Biological Evaluation Execution & Authorship Training

Biocompatibility for Medical Devices

Clinical Evaluations and Investigations & Performance Evaluations

European Medical Device Regulations

In Vitro Diagnostic Regulations

In Vitro Diagnostic Workshop: Compiling and Completing Technical Documentation

MedTech Showcases

Medical Device Law and Compliance

Post-Market Surveillance and Vigilance

Project Management Training Course

Regulatory Affairs in Global Markets: APAC Region

Regulatory Affairs in Global Markets: US Region

Software and AI for Medical Devices & IVDs

Day Three – 12 June 2024Wednesday, 12 June 2024 - CEST (Cent Europe Summer, GMT+2)

Streams

Biocompatibility Workshop: Biological Evaluation Execution & Authorship Training

Biocompatibility for Medical Devices

Clinical Evaluations and Investigations & Performance Evaluations

European Medical Device Regulations

In Vitro Diagnostic Regulations

In Vitro Diagnostic Workshop: Compiling and Completing Technical Documentation

MedTech Showcases

Medical Device Law and Compliance

Post-Market Surveillance and Vigilance

Project Management Training Course

Regulatory Affairs in Global Markets: APAC Region

Regulatory Affairs in Global Markets: US Region

Software and AI for Medical Devices & IVDs

PreviousPrevDay Two – 11 June 2024Tuesday, 11 June 2024

NextDay Four – 13 June 2024Thursday, 13 June 2024

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Streams

Biocompatibility Workshop: Biological Evaluation Execution & Authorship Training

Biocompatibility for Medical Devices

Clinical Evaluations and Investigations & Performance Evaluations

European Medical Device Regulations

In Vitro Diagnostic Regulations

In Vitro Diagnostic Workshop: Compiling and Completing Technical Documentation

MedTech Showcases

Medical Device Law and Compliance

Post-Market Surveillance and Vigilance

Project Management Training Course

Regulatory Affairs in Global Markets: APAC Region

Regulatory Affairs in Global Markets: US Region

Software and AI for Medical Devices & IVDs

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Download Agenda
Day One – 10 June 2024
Day Two – 11 June 2024
Day Three – 12 June 2024
Day Four – 13 June 2024
Day Five – 14 June 2024

#MedTech

MedTechIC
MedTech: Regulation & Strategy
Medical Device Regulatory Affairs

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