MedTech Academy

Emne

Aktivitetstype

Dato

Sprog

Corrective & Preventive Actions (CAPA)

FDA Regulation of Medical Devices: Recent FDA Guidance Documents

Process Validation

Reimbursement as a Driver for Commercial and Clinical Strategies

Industrial Sterilization of Medical Devices

IEC 62304: Software Lifecycle

Introduction to the IVDR for CE Marking

Introduktion til UDI (Unique Device Identification) - Identifikation og mærkning af medicinsk udstyr

Biocompatibility Under the New ISO 10993-1: Practical Strategies and Case Studies

Person Responsible for Regulatory Compliance according to MDR and IVDR

Introduction to MDR (2017/745)

Digital markedsføring af medicinsk udstyr

Combination Products - Regulatory & Quality Introduction

MDR Auditing - Training of Internal Auditors in Relation to MDR

IEC 62304: Software Lifecycle

Seminar for regionale indkøbere og leverandører for medicinsk udstyr

Secure Health Software Development Through IEC 81001-5-1 Compliance

IEC 60601 - How to Apply Safety and Risk Management to Medical Electrical Equipment and Systems

Introduction to Polymer Materials in Medical Devices - from a Biocompatibility Risk Perspective

FDA Regulation of Medical Devices: Recent FDA Guidance Documents

Training of internal auditors in relation to country specific requirements within the MDSAP program

Introduktion til medicobranchen

Process Validation

MedTech RA Officer - Kan købes individuelt til test

Modul 1: Anatomi, fysiologi & sygdomslære - TEST enkeltkøb

Modul 1: Anatomi, fysiologi & sygdomslære - TEST modulkøb

Anatomi, fysiologi & sygdomslære

ISO 13485 and Quality Management for Medical Devices / Internal Auditing

Clinical Evaluation and Investigation for Medical Devices: ISO 14155 and ISO 18969

Medical Device Usability

Project Management for Product Development of Medical Devices

Design Control

Modul 2: Det europæiske godkendelsessystem for medicinsk udstyr og medicinsk udstyr til in vitro-diagnostik - TEST enkeltkøb

Modul 2: Det europæiske godkendelsessystem for medicinsk udstyr og medicinsk udstyr til in vitro-diagnostik - TEST modulkøb

Det europæiske godkendelsessystem for medicinsk udstyr i henhold til MDR og IVDR

Praktisk gennemførsel af risikoanalyser ved produktudvikling

MDSAP Fundamentals and Readiness Training

Introduktion til udbudsloven

Medico virksomheders behandling af personoplysninger – juridiske og praktiske udfordringer

MDR Compliance of Medical Devices Incorporating AI/ML Algorithms

Modul 3: Materialer og klinisk evaluering - TEST enkeltkøb

Modul 3: Materialer og klinisk evaluering - TEST modulkøb

Software as Medical Device and Quality Management

Eksamen

Eksamen - TEST enkeltkøb

Introduction to Security Risk Management for SW96 and TIR57 Compliance

Person Responsible for Regulatory Compliance according to MDR and IVDR

Introduktion til UDI (Unique Device Identification) - Identifikation og mærkning af medicinsk udstyr

Digital markedsføring af medicinsk udstyr

The New US Quality Management System Regulation (QMSR)

New update on China NMPA Regulation and Registration or Medical Devices

IEC 60601 - How to Apply Safety and Risk Management to Medical Electrical Equipment and Systems

Process Validation

Introduktion til medicobranchen

Project Management for Product Development of Medical Devices

ISO 13485 and Quality Management for Medical Devices / Internal Auditing

Clinical Evaluation for Medical Devices in Europe and International approach

Sundhedssystemets opbygning & Market Access

Design Control

Medical Device Usability

Industrial Sterilization of Medical Devices - An Introduction to the Practical Approach of Sterilization

Introduktion til udbudsloven

Reimbursement as a Driver for Commercial and Clinical Strategies

Threat Modelling, Security Architecture and Controls for Medical Devices: Attacking and Defending

Dato ikke angivet

MedTech RA Officer - Modulopbygget til test

Kontakt

Berit Munkebo

Berit Munkebo

Udviklingschef

Tlf. 49184708
Mail: bm@medicoindustrien.dk