100% free · Certified

Medical device free training with certification

ISO 13485 · EU MDR · ISO 14971 · FDA QMSR · CDSCO

19

Courses

290

Modules

19

Exams

How certification works

Verify →
01

Study

Plain-language modules mapped to clauses.

02

Exam

Timed exam · 80% to pass · retake anytime.

03

Certificate

Instant, with a unique verifiable ID.

SkillMed Pro programmes

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More free courses

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Explore

Learning categories

Pick the regulatory area you work in — every track is free and certified.

No paywalls, ever

Every course, exam and certificate is free.

19 certifying exams. No credit card, no cohort dates, no proctoring fees — create a free account and start reading in under a minute.

Why SkillMed

Built for working quality & regulatory professionals.

A teaching-first academy: read, be assessed, be certified — with content maintained against the current standards.

19 courses

290 modules of structured reading material, all free.

About the academy
  • Free with certification

    Every course, exam and personalised certificate is free. No paywalls, no hidden fees.

  • Clause-by-clause material

    Structured around the actual requirements of each standard — focused, plain-language modules.

  • Timed, randomised exam

    Simulates real assessment conditions with an 80% pass mark and unlimited retakes.

  • Instant verifiable certificate

    Generated the moment you pass, with a unique ID ready for HR and quality records.

  • Standards-aligned

    Mapped to the ISO, EU and FDA requirements your teams are actually audited against.

  • Learn on any device

    No installs, no proctoring fees, no waiting for cohorts — study anywhere, any time.

Learner stories

What learners say

Reviews left by professionals after passing the certifying exam.

Reference shelf

Free regulatory resources

Official guidance from the regulators themselves — curated and always free to download.

IMDRF

4 documents

International Medical Device Regulators Forum — global convergence guidance, all free to download.

Open library

GHTF (legacy)

1 documents

Global Harmonization Task Force final documents — superseded by IMDRF but still widely referenced.

Open library

EU MDR / IVDR / MDCG

4 documents

European Commission — regulations and MDCG guidance for medical devices and IVDs.

Open library

Indian MDR / CDSCO

1 documents

Central Drugs Standard Control Organisation — India's regulator for medical devices.

Open library

US FDA / CDRH

4 documents

US Food and Drug Administration — Center for Devices and Radiological Health.

Open library

ISO / IEC reference

6 documents

Official overview pages for key standards. Full standards are paid — overviews are free.

Open library

WHO & other regulators

7 documents

Global health body and major national regulators.

Open library

The Journey

Your learning path

A structured process from reading to official certification.

1. Study Modules

Plain-language, clause-mapped modules.

2. Pass Exam

80% score required to qualify.

3. Get Certified

Instant verifiable certificate.

4. Apply Skill

Ready for audits and projects.

Help centre

Common questions

Is SkillMed really free?

Yes — every self-paced course, exam and certificate is 100% free.

Do I get a certificate?

Yes — a personalised certificate is generated instantly the moment you pass with 80% or higher.

What is the passing criteria?

All assessments require a minimum score of 80%.

Can I retake the exam?

Yes — review the modules and try again any time, at no cost.

Trusted globally

SkillMed by the Numbers

Real learners, real certificates — a growing community of medical device professionals.

3,300+
Learners
3,550+
Certificates Issued
19+
Courses Available
290+
Learning Modules