Skip to content

We use cookies needed for the site to work and, if you accept, others to measure use and improve our communications. You can change your choice at any time. See the details

Diploma program · Quality for medical devicesISO 13485:2016

Quality that protects the people who use the device.

Program under reviewAsk about availability

4,9/5641 reviews on GoogleSee reviews

G-CERTI · GLOBAL CERTIFICATION

YOUR PROFESSIONAL BACKGROUND

Present your training. Share a verifiable professional record.

Two academic certificates. The same person.

Each diploma program awards two academic certificates after its assessments are passed: system design and internal auditing. Each document retains its standard, edition and completed stage.

Each completed assessment adds to your record.

Learn about registration

Your profile in the G-CERTI Professional Directory is published after your background is reviewed and with your specific consent. View the professional directory

Where to apply what you learn

ISO 13485 organizes quality in the design, manufacture and traceability of medical devices.

31.215

ISO 13485 management system certificates worldwide · Global adoption 2024ISO Survey 2024 · G-CERTI observatory
2016Current edition · ISO 13485:2016, confirmed by ISO in 2025Current edition · ISO 13485:2016
Illustrative image

Where it applies

Where it applies

Manufacturing · Manufacturers of medical equipment and devices.

Your professional contribution

Controls at every manufacturing stage.

  • Manage product risks
  • Validate processes
  • Control changes

Examples of areas of application. Each position has its own training and experience requirements.

See sources and context

The ISO Survey 2024 counts management system certificates by standard, not jobs or graduates. Its coverage changed with the use of IAF CertSearch, so we do not present comparisons with previous years.

ISO Survey 2024 · G-CERTI observatory · ISO methodology. The images in this section are illustrative.

How the training is rated

Swipe to explore · 1/5
4,9/5641 reviews on GooglePublished institutional rating · G-CERTI LATAMSee on Google
  • “Excelente institución con una calidad educativa y humana sobresaliente.”
    Nicolás CernadasExperience with G-CERTI · Institutional review
  • “La atención de los asesores de cuenta es muy cordial.”
    Yamil MaidanaExperience with G-CERTI · Institutional review
  • “Excelente la calidad de gente. El profesor Alfredo, un genio.”
    Andrea MoralesExperience with G-CERTI · Institutional review
  • “Excelente formación y disposición para enseñar.”
    Noelia RojasExperience with G-CERTI · Institutional review
  • “Excelente experiencia.”
    Estrella CarizzaExperience with G-CERTI · Institutional review

Public Google reviews of G-CERTI LATAM, quoted verbatim. They rate the experience with G-CERTI; they do not refer to a particular cohort.

We answer your questions

Before choosing your training.

Ask on WhatsApp
When will the ISO 13485 diploma program open?

The program is under academic review. Ask about availability and we will let you know when there is a confirmed intake.

Which edition is covered?

The reference is ISO 13485:2016, an edition confirmed by ISO in 2025.

Can I start with another diploma program?

Yes. You can explore the available diploma programs, such as ISO 9001, while the ISO 13485 program is under review.

Ask about ISO 13485 availability

We will let you know when the program has a confirmed intake.

Official channel · WhatsApp +54 9 11 2299-2087