"MedStandart" offers professional training programs in technical regulation within the European Union. We’ll help you and your team acquire the essential knowledge needed for success in the European market for medical devices.

What we offer:

• Consultations and training on international standards:

• ISO 9001 — quality management systems.
• ISO 19011 — auditing management systems.
• ISO 13485 — standards for medical devices.

EU trade legislation:
In-depth understanding of regulatory requirements, including MDR 2017/745 and working with

Who our courses are for:

Our programs are designed for professionals aiming to deepen their knowledge and become experts in certification, standards, and regulation of medical devices. Regardless of your experience, we’ll tailor the training to your needs — from beginners to seasoned professionals.

Why choose us:

Practical knowledge:Training is based on real-world experience working with European regulators.

Personalized approach: Flexible formats — in-person, online, or hybrid courses.

Certificates:Upon completion, you’ll receive documents confirming your skills and competencies.

Expert team: Our trainers are specialists with years of experience in certification and regulation.

How it works:

1. Contact us: Submit a request or call to discuss your needs.

2. Choose a program:We’ll select a course perfectly suited to your company or team.

3. Attend training:Participate in interactive sessions with practical examples.

4. Become an expert: Gain knowledge and a certificate for confident market entry into the EU.

Ready to upskill? Contact us!
Contacts::

• Phone: +48791063674
  Email: This email address is being protected from spambots. You need JavaScript enabled to view it.