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ISO 13485 – Where to Start?

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ISO 13485 – Where to Start? - Advisera

ISO 13485 & EU MDR Documentation Toolkits

All of the key ISO 13485 and EU MDR documents, records, and templates necessary to complete your certification process.

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ISO 13485 – Where to Start? - Advisera

ISO 13485 Trainings

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Implementation

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Purchasing controls in ISO 13485 – Why are they needed, and what are the requirements?

by Kristina Zvonar Brkic

ISO 13485 implementation

by Waqas Imam

Calibration requirements in ISO 13485

by Anita Joshi

How to comply with ISO 13485:2016 requirements for handling complaints

by Waqas Imam

Using ISO 13485 to manage process validation in the medical device manufacturing industry

by Waqas Imam

How to perform management review according to ISO 13485

by Strahinja Stojanovic

How to manage design and development of medical devices according to ISO 13485:2016

by Waqas Imam

How to comply with section 8.2 Monitoring and measurement in ISO 13485:2018

by Verlene Law

Managing cleanliness of a product and contamination control according to ISO 13485:2016

by Waqas Imam

How to manage recalls and advisory notices for medical devices according to ISO 13485

by Waqas Imam

How to define roles and responsibilities within an ISO 13485-based QMS

by Strahinja Stojanovic

Documentation

Validation Master Plan for medical devices: Do you need it, and how to create it under ISO 13485?

by Kristina Zvonar Brkic

List of mandatory documents required by ISO 13485:2016

by Strahinja Stojanovic

Common mistakes with ISO 13485:2016 documentation control and how to avoid them

by Verlene Law

How to write a good ISO 13485 Quality Policy

by Kristina Zvonar Brkic

ISO 13485: How to write a short quality manual

by Waqas Imam

How to meet ISO 13485:2016 requirements for medical device files

by Waqas Imam

How to structure Quality Management System documentation according to ISO 13485

by Waqas Imam

How to write clinical evaluation reports under the EU MDR

by Kristina Zvonar Brkic

How to manage the Quality Manual according to ISO 13485:2016 requirements

by Waqas Imam

Internal audit

Five main steps in the ISO 13485:2016 internal audit

by Waqas Imam

How to perform a supplier audit according to ISO 13485

by Kristina Zvonar Brkic

How to create a checklist for an ISO 13485 internal audit for your QMS

by Waqas Imam

First-, Second- & Third-Party Audits for medical device manufacturers & suppliers

by Waqas Imam

General

How to get ISO 13485 certified?

by Kristina Zvonar Brkic

Differences and similarities between FDA 21 CFR Part 820 and ISO 13485

by Waqas Imam

ISO Enabled Free Access to ISO 13485 and Other Medical Device and Protective Clothing Standards

by Liza Horielikova

Medicines and Healthcare products Regulatory Agency in the UK – What does it do and how can ISO 13485 help?

by Waqas Imam

How to perform ISO 13485 training

by Kristina Zvonar Brkic

Setting good quality objectives for ISO 13485

by Waqas Imam

How to choose a consultant for ISO 13485 implementation

by Chany Runnels

List of worldwide regulations that require implementation of ISO 13485

by Kristina Zvonar Brkic

Plan-Do-Check-Act in the ISO 13485 standard

by Waqas Imam

How can ISO 13485 help manufacturing companies?

by Kristina Zvonar Brkic

Infographic: What’s new in the 2016 revision of ISO 13485

by Strahinja Stojanovic

EU MDR

EU MDR – Detailed Explanation

by Kristina Zvonar Brkic

PMCF: How to run a post-market clinical follow-up according to the MDR

by Kristina Zvonar Brkic

EU MDR Step-by-Step Implementation Guide for Medical Devices

by: Kristina Zvonar Brkic

What are the deadlines for medical device manufacturers to comply with EU MDR?

by Kristina Zvonar Brkic

Medical device classification according to the EU MDR

by Kristina Zvonar Brkic

Comparison of the EU MDR and IVDR regulations

by Kristina Zvonar Brkic

EU MDR – Easy-to-understand basics

by Mark Hammar

How to comply with the MDR requirements for medical device labels

by Kristina Zvonar Brkic

Steps to transition from the EU MDD to the MDR

by: Kristina Zvonar Brkic

Similarities and differences between the EU MDR and UK MDR.

by Kristina Zvonar Brkic

What are The EU MDR Technical Documentation Structure and Requirements?

by Kristina Zvonar Brkic

Infographic: EU MDR vs. MDD – What has changed?

by Kristina Zvonar Brkic

What are the post-market surveillance requirements in the MDR?

by Kristina Zvonar Brkic

What are economic operators’ roles and responsibilities under the MDR?

by Kristina Zvonar Brkic

How can ISO 13485 help with MDR compliance?

by Kristina Zvonar Brkic