ISO 13485 Webinars

If you are a quality management professional responsible for maintaining or implementing the quality management system for medical devices sector, and you are not sure where to begin or how to comply with ISO 13485, our webinars (online trainings) are the perfect solution for you.

Online Trainings via Webinar

A How-to Guide for ISO 13485 Implementation [free webinar]

Available as: Live webinar, Webinar on demand

Date: Thursday - February 9, 2023

class="time-container ">Time: 8:00 PM (Convert to your time zone)

Webinar designed for companies that are planning to implement ISO 13485, and don’t have much experience with the standard. This webinar will help you understand what kind of standard ISO 13485 is, what the basic terms are, and what the implementation process looks like.


How to perform an ISO internal audit [free webinar]

Available as: Live webinar, Webinar on demand

Date: Thursday - February 16, 2023

class="time-container ">Time: 11:00 AM (Convert to your time zone)

All ISO management standards, together with the IATF 16949 and AS9100 standards, require the use of internal audits as a performance evaluation tool. This webinar will help you answer all your questions and doubts while preparing to perform an internal audit, and give you insights on how to execute it.


How To Use a Documentation Toolkit To Implement EU MDR and ISO 13485 [free webinar on demand]

Available as:

Date: Wednesday - February 21, 2018

class="time-container ">Time: 5:00 PM (Convert to your time zone)

Webinar designed for companies that are planning to implement EU MDR and ISO 13485 using the do-it-yourself approach. During this webinar, you will be able to see whether the templates, know-how, and support from Advisera’s 13485Academy are applicable to your implementation project.


Understanding the Process of Clinical Evaluation Under EU MDR for Beginners [Free Webinar on Demand]

Available as: Webinar on demand

Date: Thursday - December 15, 2022

class="time-container hideWebinarDateClass">Time: 8:00 PM (Convert to your time zone)

The purpose of the webinar is to familiarize the participants with the basics of how to conduct the clinical evaluation.


How To Perform Consulting Work Remotely [free webinar on demand]

Available as: Webinar on demand

Date: Wednesday - May 20, 2020

class="time-container hideWebinarDateClass">Time: 5:00 PM (Convert to your time zone)

Webinar designed for consultants for ISO 9001, ISO 14001, ISO 27001, and other ISO management standards. The webinar explains how perform consulting services when working remotely, i.e., from home or other off-site locations.


Overview of the Steps Needed to Comply With EU MDR [free webinar on demand]

Available as: Webinar on demand

Date: Tuesday - March 2, 2021

class="time-container hideWebinarDateClass">Time: 8:00 PM (Convert to your time zone)

Webinar designed for organizations that have medical devices that need to be certified according to the EU MDR. This webinar will help you understand the necessary steps that need to be taken, and requirements to be fulfilled, to be fully prepared when the MDR takes full effect (May 2021).


ISO 14971:2012 – How To Conduct Risk Management for Medical Devices [free webinar on demand]

Available as: Webinar on demand

Date: Thursday - December 12, 2019

class="time-container hideWebinarDateClass">Time: 5:00 PM (Convert to your time zone)

Webinar designed to familiarize the participants with the basics of risk management for medical device manufacturers, and to explain necessary concepts so that participants know how to implement risk management themselves.


Understanding the European Medical Device Regulation and How ISO 13485 Supports It [free webinar on demand]

Available as: Webinar on demand

Date: Wednesday - March 17, 2021

class="time-container hideWebinarDateClass">Time: 8:00 PM (Convert to your time zone)

Webinar designed to familiarize the participants with the basics of the new EU MDR regulation for medical devices, and how ISO 13485 can speed up the compliance process.


Cómo realizar una auditoría interna en remoto [webinar a pedido gratis]

Available as: Webinar on demand

Date: Thursday - November 19, 2020

class="time-container hideWebinarDateClass">Time: 5:00 PM (Convert to your time zone)

Este seminario web está dirigido a auditores internos de ISO 9001, ISO 14001 e ISO 27001, así como otros sistemas de gestión ISO. Este seminario web explica qué diferencias y cambios existen en comparación con una auditoría presencial, pero también trata los riesgos y obstáculos que deben de considerarse, tanto durante la preparación y realización de una auditoría interna en remoto.


How To Sell ISO Consulting Services [free webinar on demand]

Available as: Webinar on demand

Date: Wednesday - April 11, 2018

class="time-container hideWebinarDateClass">Time: 5:00 PM (Convert to your time zone)

Webinar designed for consultants for ISO 9001, ISO 14001, ISO 27001, and other ISO management standards. The webinar explains how to sell your knowledge in this very competitive market.


How To Perform an Internal Audit Remotely [free webinar on demand]

Available as: Webinar on demand

Date: Thursday - February 4, 2021

class="time-container hideWebinarDateClass">Time: 8:00 PM (Convert to your time zone)

Webinar designed for internal auditors for ISO 9001, ISO 14001, ISO 27001, and other ISO management standards. The webinar explains what changes must be made, and what risks and obstacles must be considered during the preparation, performance, and reporting of a remote internal audit.


What Has Changed in the IVD Industry After EU IVDR – Challenges and Implementation [free webinar on demand]

Available as: Webinar on demand

Date: Tuesday - October 26, 2021

class="time-container hideWebinarDateClass">Time: 5:00 PM (Convert to your time zone)

Webinar designed for all stakeholders involved in the process of adherence to the European Commission's (EC) In Vitro Diagnostic Regulation (EU IVDR 2017/746) requirements. That includes manufacturers, suppliers, notified bodies, competent authorities, authorised representatives, importers, etc.