Veranex regularly offers online training on a wide range of MedTech topics. Our subject matter experts deliver interactive sessions in small groups, tapping into real examples from our 20+ years of experience to provide you with the industry’s latest updates and best practices.
Upcoming Training
Training: ISO 14155:2020 Clinical Investigation of Medical Devices for Human Subjects — Good Clinical Practice
March 11 & 13 2025, Online
6 hours | 2 x 9:00 – 12:00 AM US Eastern Standard Time, 2 x 3:00 – 6:00 PM Central Europe Time
Training: EU General Data Protection Regulation (EU GDPR)
March 20, 2025, Online
4 hours | 8:00 – 12:00 AM US Eastern Standard Time, 2:00 – 6:00 PM Central Europe Time
Training: Basic Biocompatibility Practical Perspective & Regulatory Aspects
April 8 & 11 2025, Online
6 hours | 2 x 8:00 – 11:00 AM US Eastern Daylight Time, 2x 2:00 – 5:00 PM Central Europe Summer Time
UK Medical Device Regulations – Understand the Regulatory Landscape of one of the largest Medical Device markets in Europe
November 30th 2023, Online
4 hours | 8:00 AM – 12:00 AM (EST), 2:00 PM – 6:00 PM (CET)
Medical Device Software And Life Cycle Processes (IEC62304)
December 12th & 14th 2023, Online
6 hours | 2x 8:00 – 11:00 AM (EST), 2:00 – 5:00 PM (CET)
Understanding the EU Regulatory Landscape for Software as Medical Device (SaMD)
March 5th 2024, Online
4 hours | 7:00 AM – 11:00 AM (EST), 1:00 PM – 5:00 PM (CET)
Cybersecurity for Medical Devices: Crash Course
January 22 – 26th 2024, Online
16:30 hours | 5x 9:00 AM – 12:30 PM (EST), 2:00 PM – 5:30 PM (CET)
Introduction to MDSAP (Medical Device Single Audit Program)
January 31st 2024, Online
4 hours | 7:00 – 11:00 AM (EST), 1:00 – 5:00 PM (CET)
Basic Biocompatibility – Practical Perspective & Regulatory Aspects
February 20th & 22nd 2024, Online
6 hours | 2x 8:00 – 11:00 AM (EST), 2:00 – 5:00 PM (CET)
Clinical Investigation of Medical Devices — Requirements of ISO 14155:2020 – Good Clinical Practice
February 28th & 29th 2024, Online
6 hours | 2x 9:00 – 12:00 AM (EST), 3:00 – 6:00 PM (CET)
Past Training
EN ISO 13485:2016 – Quality Management System (QMS)
This training currently has no open sessions. If you would like to attend, please leave us a message, and we will inform you when a new date is planned. Training Objectives: Understand the QMS principles and the links between the different QMS processes Define...
Overview of the PMS and PMCF requirements under the Medical Device Regulation (MDR)
This training currently has no open sessions. If you would like to attend, please leave us a message, and we will inform you when a new date is planned. Training Objectives: Understand Post Market Surveillance (PMS) & Post Market Clinical Follow-up (PMCF)...
Electrical Safety
This training currently has no open sessions. If you would like to attend, please leave us a message, and we will inform you when a new date is planned. Training Objectives: Gain a general understanding of IEC 60601 standards (collateral and particular...
Cybersecurity
This training currently has no open sessions. If you would like to attend, please leave us a message, and we will inform you when a new date is planned. Training Objectives: This training is intended to allow the participants to understand the requirements...
Substance-based Device Regulation
This training currently has no open sessions. If you would like to attend, please leave us a message, and we will inform you when a new date is planned. Training Objectives: The goal of this training is to provide participants with an introduction to substance-based...
EUDAMED
This training currently has no open sessions. If you would like to attend, please leave us a message, and we will inform you when a new date is planned. Training Objectives: Understand EUDAMED and its functional specifications Interpret EUDAMED data...
Person Responsible for Regulatory Compliance (PRRC) – EU & Swiss Regulations
This training currently has no open sessions. If you would like to attend, please leave us a message, and we will inform you when a new date is planned. Training Objectives: Understand the regulatory context of PRRC roles and responsibilities in both EU and CH...