Postgraduate DiplomaDefense, Military Engineering & Land Systems Applications open

Diploma in Validation of Military Medical Systems

Online postgraduate diploma of 800 hours in the validation of military medical systems. 8 modules covering medical devices in defence, risk and quality management to ISO 14971 and ISO 13485, design verification to IEC 60601-1, military environmental testing to MIL-STD-810H, clinical and usability validation, connected devices and regulation, with an assigned technical tutor.

Duration6–8 months
ModeOnline
LanguageEnglish
Start datesSet by the faculty
AwardSEIUM Institute diploma

Diploma in Validation of Military Medical Systems — studying from Canada

Canada's defence sector is centred on procurement and sustainment through the Department of National Defence and Defence Research and Development Canada. Industrial activity spans land vehicles, naval systems, avionics and electronics, with firms in Ontario, Québec, Nova Scotia and British Columbia. Companies such as General Dynamics Land Systems Canada and Lockheed Martin Canada are notable employers, alongside a broad base of small and medium suppliers. Engineers work on systems integration, vehicle protection, logistics and sustainment, operating within strict security and export control frameworks.

Fees for Canada: C$2,330 (Canadian dollar), with instalments and employer sponsorship available.

Relevant bodies in Canada

  • Department of National Defence (DND)
  • Defence Research and Development Canada (DRDC)
  • Canadian Association of Defence and Security Industries (CADSI)
  • Public Services and Procurement Canada

Typical roles

  • Defence Systems Engineer
  • Land Systems Engineer
  • Systems Integration Engineer
  • Sustainment Engineer

Questions from Canada

Which Canadian bodies or processes govern defence engineering recognition?

Defence engineering in Canada often involves government procurement and security clearances, and engineers typically hold provincial Professional Engineer licences where a title is required. SEIUM's qualifications are private and not official state degrees or accredited by a national body, so they do not confer licensing or clearance. Recognition is for employers or the relevant body to decide, so verify this first.

Would Canadian defence or land systems employers accept this training?

Canadian defence employers and contractors generally rely on security clearance, licensing and demonstrated experience. A private qualification may support your application, but it is unlikely to replace those requirements, and its acceptance is up to each employer. A SEIUM final project can help show applied skill, so discuss expectations with prospective employers early.

Can I study remotely while working, and what are the costs and language demands?

Yes, the programmes are fully online, so you can study from Canada or elsewhere without a student visa, and fit sessions around work. Specialist courses are 300 hours, postgraduate diplomas 800 and master's 1,900. Teaching is in English, supported by an assigned technical tutor. Fees are payable in instalments, and employer sponsorship may be available.

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Learning outcomes

What you will be able to do

01

Understand the requirements for medical devices in defence.

02

Apply risk and quality management systems.

03

Plan design verification in line with standards.

04

Design environmental tests for military environments.

05

Validate usability and clinical performance.

06

Validate software and connected medical devices.

07

Apply the regulatory and ethical framework to procurement.

Profile

Who it's for

  • Medical device validation engineers moving into military healthcare.
  • Regulatory affairs specialists handling CE marking and MDR compliance.
  • Biomedical engineers working on field and transport equipment.
  • Healthcare quality managers responsible for ISO 13485 systems.
  • Environmental test engineers applying MIL-STD-810H to medical equipment.
  • Usability specialists testing devices with clinical users.
  • Engineering or science graduates seeking to enter military healthcare.
Standards & tools

What you'll work with

  • Regulation (EU) 2017/745 (medical devices)
  • ISO 13485:2016 (quality management systems for medical devices)
  • ISO 14971:2019 (risk management for medical devices)
  • IEC 60601-1 (safety of medical electrical equipment)
  • MIL-STD-810H (environmental engineering considerations and laboratory tests)
  • IEC 62366-1 (usability engineering)
  • IEC 62304 (medical device software life cycle)
  • Greenlight Guru
  • MATLAB
  • LabVIEW
  • Jama Connect
  • Python SciPy
Syllabus

8 modules

  1. 1.1Military medicine and medical equipment
  2. 1.2Medical devices in austere environments
  3. 1.3Field and evacuation equipment
  4. 1.4Devices on aircraft and ships
  5. 1.5Extreme environmental requirements
  6. 1.6Classification of medical devices
  7. 1.7The European Medical Device Regulation
  8. 1.8Exemptions and emergency use
  9. 1.9Product life cycle
  10. 1.10Case study: requirements for a transport ventilator
  1. 2.1ISO 14971 risk management
  2. 2.2ISO 13485 quality management
  3. 2.3Clinical hazard analysis
  4. 2.4Design controls
  5. 2.5Requirements traceability
  6. 2.6Supplier management
  7. 2.7Corrective and preventive actions
  8. 2.8Quality audits
  9. 2.9Technical documentation
  10. 2.10Workshop: risk analysis of a patient monitor
  1. 3.1Verification plan
  2. 3.2Electrical safety to IEC 60601-1
  3. 3.3Electromagnetic compatibility to IEC 60601-1-2
  4. 3.4Transport equipment to IEC 60601-1-12
  5. 3.5Essential performance
  6. 3.6Software testing to IEC 62304
  7. 3.7Biocompatibility to ISO 10993
  8. 3.8Packaging tests
  9. 3.9Test reports
  10. 3.10Laboratory: electrical safety test
  1. 4.1MIL-STD-810H and its application
  2. 4.2Vibration and shock
  3. 4.3Temperature and humidity
  4. 4.4Altitude and decompression
  5. 4.5Sand, dust and rain
  6. 4.6Aircraft compatibility to RTCA DO-160
  7. 4.7Drop tests
  8. 4.8Mission profiles
  9. 4.9Test tailoring
  10. 4.10Practical exercise: environmental test plan for a defibrillator
  1. 5.1Validation versus verification
  2. 5.2Clinical evaluation
  3. 5.3Clinical investigations to ISO 14155
  4. 5.4Usability engineering to IEC 62366
  5. 5.5Testing with healthcare users
  6. 5.6Use with protective equipment
  7. 5.7Clinical simulation
  8. 5.8Validation in realistic scenarios
  9. 5.9Ethics of clinical research
  10. 5.10Case study: usability validation of a tourniquet
  1. 6.1Software as a medical device
  2. 6.2IEC 62304 life cycle
  3. 6.3Medical device cybersecurity
  4. 6.4Clinical data interoperability
  5. 6.5Artificial intelligence in diagnosis
  6. 6.6Algorithm validation
  7. 6.7Software updates
  8. 6.8Patient data management
  9. 6.9Telemedicine and devices
  10. 6.10Laboratory: validation of an alarm algorithm
  1. 7.1CE marking and notified bodies
  2. 7.2Post-market surveillance
  3. 7.3Procurement of military medical equipment
  4. 7.4Medical STANAGs
  5. 7.5Allied medical interoperability
  6. 7.6Legal liability
  7. 7.7Military medical ethics
  8. 7.8Equitable access to technology
  9. 7.9Lessons from the pandemic
  10. 7.10Case study: equipment procurement file
  1. 8.1Definition of the device
  2. 8.2Risk analysis
  3. 8.3Verification plan
  4. 8.4Environmental test plan
  5. 8.5Clinical validation plan
  6. 8.6Usability plan
  7. 8.7Regulatory strategy
  8. 8.8Conclusions
  9. 8.9Report and presentation
  10. 8.10Final project: final review with the tutor
Methodology, software & labs

How you'll learn

The programme is delivered 100% online on the SEIUM campus, with downloadable material, recorded classes and an assigned technical tutor. There are no fixed timetables: you progress at your own pace within each intake, so it can be combined with your job.

Each module combines theory, guided reading of the original standard and applied exercises. The working software is Greenlight Guru, MATLAB, LabVIEW, Jama Connect and Python SciPy, in free, academic or evaluation versions. Testing is studied through real procedures for electrical safety tests, vibration and temperature environmental tests and usability tests with healthcare professionals. Assessment is continuous by module, plus the final project.

Standards covered: Regulation (EU) 2017/745, ISO 13485:2016, ISO 14971:2019, IEC 60601-1, MIL-STD-810H, IEC 62366-1 and IEC 62304.

Assigned technical tutor:every module ends with a deliverable that your tutor marks individually.
Standards-based learning:guided reading of Regulation (EU) 2017/745, ISO 13485:2016 and ISO 14971:2019 applied to real cases, not as a theoretical annex.
Industry software:Greenlight Guru, MATLAB, LabVIEW, Jama Connect and Python SciPy, in free, academic or evaluation versions.
Final project:a complete validation plan for a military medical device covering risk analysis, verification, environmental testing, clinical validation, usability and regulatory strategy, reviewed by your tutor.
Flexible format:100% online, no fixed timetables, compatible with full-time work.
Capstone project

Build it end to end

Your final project follows the real engineering workflow, step by step, reviewed by your tutor.

Risk analysis
Carry out an ISO 14971 risk analysis of a patient monitor.
Electrical safety testing
Plan and evaluate an IEC 60601-1 electrical safety test.
Environmental test plan
Draw up a MIL-STD-810H environmental test plan for a defibrillator.
Usability validation
Validate the usability of a tourniquet with clinical users.
Final project
Develop a complete validation plan for a military medical device, reviewed by your tutor.
Career opportunities

Where this takes you

Medical Device Validation EngineerRegulatory Affairs SpecialistBiomedical EngineerHealthcare Quality ManagerEnvironmental Test EngineerUsability Specialist
Admissions & scholarships

Requirements

  • Prior technical training or professional experience in the sector. No university degree is required.
  • An internet connection and a computer capable of running the programme software.
  • English sufficient to read technical standards.

Ready to start?

Send your application today. Our admissions team replies within 72 hours with your study plan and funding options.

FAQ

Frequently asked questions

The programme totals 800 hours over 6–8 months. You set your own pace within each intake, and your tutor helps you plan the workload around your job.

You work with Greenlight Guru, MATLAB, LabVIEW, Jama Connect and Python SciPy, using free, academic or evaluation versions. Your tutor indicates the free alternative wherever one exists.

A SEIUM Institute diploma, awarded on passing the continuous assessment and the final project. It is SEIUM's own qualification, not an official state degree; its recognition depends on the programme completed and the regulations of each country.

Yes. Modules passed are recognised in a higher programme in the same area (postgraduate diploma or master's). Ask about the recognition policy when you enrol.

Prior technical training or professional experience in the sector (no university degree required), a computer able to run the programme software and English sufficient to read technical standards.

Start dates are set by SEIUM's faculty for each intake. Our admissions team will confirm the next available date when you apply.

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