Advance Your Expertise in Medical Device Compliance and Safety

The medical device industry is rapidly evolving, making it crucial to stay up to date with the latest regulatory frameworks and technological advancements. SIQ Ljubljana provides a comprehensive array of specialized training programs that address key topics, including ISO 13485, risk management under ISO 14971, IEC 60601-1 safety standards, and the EU Medical Device Regulation (MDR). Our courses are meticulously designed to equip manufacturers, suppliers, and industry professionals with the knowledge and skills required to ensure compliance and enhance product safety.

We are now accepting preliminary applications and encourage you to express your interest in participating via the link.

More information:
Bojan Varga
E-mail: bojan.varga@siq.si
Tel.: +386 1 7448 108