Advanced Risk Practitioner (ISO 14971) for Medical Devices

£895.00
4.5 ★★★★★ 14 Reviews
RAPS Cretified Course

Advanced Risk Practitioner Training (Medical Devices) is for anyone who wants both a comprehensive overview of the international standard for risk management for medical devices, and to acquire the best practice skills to readily apply the knowledge and tools successfully within their organization.

Our blended learning course is a hybrid approach where you first complete eLearning modules on the underlying theory that better prepares you in advance of attending Live Classes with an Instructor where Learners will work with case studies & scenarios that help deepen the understanding of the requirements, and applying the tools & techniques in a real life context.

The Regulatory Affairs Professionals Society (RAPS) recognize this course offering global recognition for successful participants and RAPS credits for members.

Advanced Risk Practitioner (ISO 14971) for Medical Devices

Overview of our Advanced Risk Practitioner (ISO 14971) Training

Approved By
Regulatory Affairs Professionals Society (RAPS)
RAPS Credits
12
Duration
18hrs
eLearning Access
90 Days
Teaching Format
Blended Learning
Course Entry Requirements
Prior knowledge is required
Certification on Completion
Issued in 1 business day
Course Content Based on
ISO 14971
Course Last Updated
February 2025
Language (s)
English
£895.00 / Seat
Sample Certificate of Advanced Risk Practitioner (ISO 14971) for Medical Devices
Trusted By Notified Bodies & Global Brands
Trusted By Notified Bodies & Global Brands
Trusted By Notified Bodies & Global Brands
Trusted By Notified Bodies & Global Brands
Trusted By Notified Bodies & Global Brands
Trusted By Notified Bodies & Global Brands

Upcoming Dates for Advanced Risk Practitioner (ISO 14971) Training

What's covered on our Advanced Risk Practitioner Training

Learners first complete interactive eLearning modules to grasp the underlying theory, then attend live, instructor-led workshops emphasizing practical, real-world application.

eLearning
  • Risk Management and Product Lifecycle
  • Risk Perception
  • Introduction to ISO 14971
  • ISO 14971:2019 Key Changes
  • Structure of ISO 14971
  • Key Terminology
  • Medical Device Regulatory Framework
  • Product and Process Standards
  • Clause 4 Overview
  • Risk Management Process
  • Risk Acceptability Policy
  • Risk Management Process Review
  • Risk Management Team Competency
  • Expert Training
  • Risk Management Plan
  • Risk Management File

Case Study! Elements of a Risk Acceptability Policy

  • Risk Assessment Overview
  • Risk Analysis Process
  • Intended Use
  • Reasonably Foreseeable Misuse
  • Safety Characteristics
  • Hazards and Hazardous Situations
  • Types of Hazards
  • Sequence of Events
  • Random & Systematic Faults
  • Risk Estimation
  • Risk Evaluation
  • Risk Analysis Tools
  • Preliminary Hazard Analysis (PHA)
  • Fault Tree Analysis (FTA)
  • Failure Mode Effect Analysis (FMEA)
  • Hazard and Operability Study (HAZOP)
  • Hazard Analysis and Critical Control Point (HACCP)

Case Study! Safety Characteristics

Case Study! Hazard Identification and Sequence of Events

  • Risk Control
  • Risk Reduction
  • Risk Control Analysis
  • Role of Standards in Risk Control
  • Implementation
  • Residual Risk Evaluation
  • Benefit-Risk Analysis
  • New Risks
  • Risk Control Completeness
  • Overall Residual Risk
  • Disclosure of Significant Residual Risks

Case Study! Benefit Risk Analysis

Case Study! Overall Residual Risk

  • Risk Management Review
  • Production and Post-Production Activities
  • Information Collected
  • Information Review
  • Actions
  • Relationship between ISO 13485 and ISO 14971
  • ISO 14971 and Design & Development

Case Study! Post-Market Surveillance and Risk

  • ISO/TR 24971 Purpose and Structure
  • ISO/TR 24971 Annexes
  • Annex F Security Risks
  • Annex H IVD Medical Devices
About our Practitioner Training
 
Live Workshops
  • Risk Management terms and definitions
  • Alignment with ISO 13485 and Regulatory Frameworks

Practical Workshop! Integrating Risk Assessment Tools into the ISO 14971 Process

  • General Requirements
  • Roles and Responsibilities in the Risk Management Process
  • Documentation Requirements: Risk Management File (RMF)

Practical Workshop! Building a Comprehensive Risk Management File (RMF)

  • Identifying hazards and hazardous situations
  • Determining foreseeable misuse
  • Conducting risk estimation
  • Tools and Techniques: FMEA, Fault Tree analysis

Practical Workshop! Using FMEA for Risk Identification and Estimation

  • Risk Acceptance Criteria

Practical Workshop! Setting and Applying Risk Acceptance Criteria

  • Risk Control Options
  • Evaluating residual risks
  • The risk-benefit analysis process

Practical Workshop! Verifying the effectiveness of Risk Control

  • Monitoring and feedback mechanisms
  • Post-market surveillance and vigilance
  • Continuous improvement in risk management

Practical Workshop! The Role of Post-market Surveillance in Risk Management

Michelle Keane

Michelle Keane

Michelle has a proven track record with over 20 years of experience working across both the Medical Device and Biotechnology sectors. Currently, she is a Lead Auditor for an INAB Accredited Certification Body, and an MDR Assessor for a Notified Body in Europe. In addition, she is the Team PRRC Representative for Ireland.
Regulatory Affairs Professionals Society (RAPS) Recognized Training
More Flexibility, More Effective & More Savings vs Other Providers
Industry-Leading Blended Learning Methodology
eLearning that Better Prepares You
Live Learning from Anywhere
Practical Workshops led by Experienced Practitioners
Tailored to your Organization

On completion of this course, successful Learners will have the practical knowledge to support their organization and apply the techniques needed to:

  1. Explain the purpose and scope of ISO 14971
  2. Outline the steps to establish, document and maintain a risk management process
  3. Analyze risk evaluation techniques and criteria in compliance with ISO 14971
  4. Apply risk control measures to reduce residual risks effectively
  5. Conduct post-market surveillance and continuous risk monitoring

This course is aimed at anyone working in the medical device sector that wants to master risk management based on ISO 14971, including:

  • Design & Development personnel
  • Quality / Engineering / Technical / Production personnel
  • Regulatory affairs
  • Internal / Lead / Supplier Auditors

RAPS Approved Provider Logo

The Regulatory Affairs Professionals Society has approved Comply Guru (No. 1007) and recognizes this course where members will be eligible for the stated number of RAPS credits (12).

Upon successful completion, each Learner shall receive a digital Certificate of Achievement within 1 business day.

Before completing this course, each Learner is recommended to have the following prior knowledge:

  • The fundamental concepts and principles of risk management as it applies to medical devices
  • The commonly used risk terms and definitions (see ISO 14971)
  • A working knowledge of ISO 13485, which may be gained by completing Comply Guru’s ISO 13485 Foundation Course

In order to successfully complete this course, each Learner will need to:

  • Complete the eLearning modules and obtain 70% or higher in the final assessment (MCQ-based)
  • Fully attend the Live Instructor Workshops as 100% attendance is required
  • Obtain 70% or higher in the graded assessments during the Live Instructor Workshops

For the live workshops during a virtual delivery, we utilize Microsoft Teams and SharePoint.

Learners need to individually have:

  • PC or MAC Computer
  • Reliable Internet
  • Video Webcam
  • Headset or Earbuds
  • Quiet Setting

In relation to the eLearning Modules, in our experience, Workplace IT environments’ internal configurations and available software can vary (new or old), and there may be various limitations or other restrictions in place, and as such, the functionality of any Learning Management System (LMS) may be impacted, restricted and may not perform well. Read the full technology requirements here.

Need Corporate, In-House or Customized Training?

Comply Guru offers corporate, in-house and customized training solutions for your organization’s specific needs.

Speak with an experienced member of our team today to learn how we can help.

Frequently Asked Questions

Blended learning is a hybrid methodology where learners first complete eLearning modules on the underlying theory in advance of Live Workshops facilitated by an experienced Instructor.

This introduces more flexibility vs traditional learning by reducing ‘fixed’ classroom hours by up to 50%. In addition, improved learner confidence & preparation from the eLearning leads to better learning outcomes during the skills-based workshops.

Yes, very practical. Our live workshops are based on the principles of Accelerated Learning (AL). AL is based on ‘learn by doing’ through practical training methods which include real-world examples, case studies, facilitated exercises and group discussions.

We are passionate about ‘No Death by PowerPoint’ or a ‘sit and listen’ methodology. In fact, there are no slides during the live workshops. Come prepared to be fully engaged and of course, to learn a lot!

Yes, we can deliver training in-person or onsite for in-company groups. However, all our public training is delivered virtually. If you prefer in-person training, get in touch, we are happy to help.

Yes, we offer in-company training provided you have 5 or more learners that can be trained together on the same dates. Please request a quote and a member of our team will be in touch to discuss this further with you.

The eLearning unlocks up to 30 days in advance of the scheduled workshop(s). This is intentional. The modules are designed for learning to be achieved in the weeks leading up to live workshop(s) to ensure continuity in learning.

Once you have successfully completed the training, including all assessments, your certificate will be available within 1 business day. To access your certificate, you must first submit a short course survey and then the certificate will be available for download/print.

Please note: no certificates are available without full payment on file.

Yes, we permit substitutions provided the license has not been activated, the substitute meets the entry criteria and there is sufficient time available for the replacement to complete the mandatory eLearning and assessments. There is no fee for substitutions.

If the workshop is delivered virtually, there will be a link on your Learner dashboard. This link will become a visible two days in advance of the start date. In addition, a calendar invite is issued.

The eLearning modules, including assessments, form a mandatory part of the training. To be eligible to attend the live workshop(s), these must be successfully completed in advance of the specific deadline date for your registered workshops(s).

Note: if the eLearning modules and assessments are not successfully completed by the deadline, you will not be eligible to attend the live workshops. No refunds are possible when you fail to complete the eLearning on time.

Yes, we permit transfers to a future date (s) provided the request is made at least 30 days in advance of the live workshops you registered for. No refund is possible if less than 30 days’ notice is given. On a case-by-case basis, if we can accommodate a transfer at less than 30-days notice, we will but this cannot be guaranteed.

Comply Guru do not provide learners with copies of international standards, nor do we require that any purchase is made. However, participants do need to have access to a copy of required standard(s) on this training.

Firstly, we suggest seeing if you can obtain a copy of the required standard(s) from a friend, colleague or at your workplace. If you are unable to do so, each country has a nominated ISO standard supplier where you may purchase the international standard(s) you need for your training.

The eLearning duration provided is an estimate based on the average amount of time it takes a learner who is new to the subject/topic. In reality, the amount of time it takes to complete the eLearning will vary depending on your prior experience, knowledge & learning style.

No, there is no end of course examination. However, you must attend 100% of the live workshops and obtain 70% or higher in graded exercises during the live workshops in order to receive certification.

Blended Learning is Better Learning

A two-step methodology with eLearning modules that help you master the theory better preparing you for practical workshops that embed the skills.
eLearning
1
MASTER THE THEORY
  • Flexible, self-paced learning
  • Minimize disruption at work
  • Modern eLearning methodology
  • Better workshop preparation
Live Learning
2
PRACTICE THE SKILLS
  • Learn-by-doing approach
  • Highly engaging workshops
  • Guidance from instructors
Qualified
3
  • Reduce training costs
  • Apply skills immediately
  • Achieve recognized outcomes

Training Transformed with Comply Guru

Comply Guru has helped organizations reduce training costs by up to 50%, accelerate workforce development, and create sustainable business value through innovative learning solutions.

What Our Learners Are Saying

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