Events

The last in a series of three webinars on risk management according to EN ISO 14971:2020 and ISO/TR 24971:2020, intended mainly for manufacturers of medical devices. This is an updated repeat of the successful online seminars held in 2023.

The webinar is designed for manufacturers who have launched their devices under previous legislation, are awaiting their first MDR certification and are unsure whether their clinical evaluation will be sufficient.

The second of three webinars on risk management according to EN ISO 14971:2020 and ISO/TR 24971:2020, intended mainly for medical device manufacturers. This is an updated repeat of the successful online seminars held in 2023.

The first of three webinars on risk management according to EN ISO 14971:2020 and ISO/TR 24971:2020, designed especially for medical device manufacturers. This is an updated repeat of the successful online seminars held in 2023.

The webinar focuses on the rules of advertising of medical devices and IVDs from the perspective of European and Czech law. You will learn how advertising to professionals differs from advertising to the general public and we will introduce you to the changes that are coming in this area.

An online seminar for all medical device suppliers considering inclusion of their products in the public health insurance reimbursement system. The aim of the seminar is to clarify basic concepts in the area of medical devices pricing and reimbursement, both in the context of voucher MDs and separately billed supplies.

The sixth annual Medical Devices Conference. This time we will conclude the last, i.e. sixth, semester of the three-year Qualification Course for persons responsible for compliance with the MDR and IVDR regulations of the Czech Agency for Standardization.

We invite you to a special webinar focused on artificial intelligence. It is intended for anyone who develops, sells or uses AI systems. In particular, we will focus on the possibilities of using AI in healthcare and in combination with medical devices.

The webinar is designed for manufacturers who have launched their devices under previous legislation, are awaiting their first MDR certification and are unsure whether their clinical evaluation will be sufficient.

The webinar is intended for all health care providers, especially small medical practices. We will present in an easy-to-understand form the basic categories of obligations, the fulfillment of which is often subject to inspections by state authorities such as the State Institute for Drug Control.

This webinar is designed for importers and distributors who want to be aware of the regulatory obligations that currently apply to them. The online seminar focuses on obligations under the European MDR and IVDR regulations, good storage practices and the basics of advertising regulation.

This webinar is designed for anyone who is interested in medical device regulation but doesn't know where to start. We will try to explain the basic concepts and processes in an easy-to-understand way. We will walk participants through the entire life cycle of a medical device in a nutshell.

The webinar is designed for manufacturers, their suppliers, importers and distributors of medical devices and IVDs who enter into quality agreements with their business partners. You will learn why it is beneficial and even mandatory to enter into such agreements and what they should contain.

Deadline to transfer appropriate surveillance to a MDR notified body for legacy devices that want to benefit from extended transition period.

Deadline to sign a written agreement with a notified body for legacy devices that want to benefit from extended transition period.