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Events

Stay up-to-date with the latest events in regulatory compliance and our agency offerings by checking out our event calendar. We offer a variety of events, including webinars, conferences, and more, to help you stay informed and improve your skills and knowledge in all medical device regulatory matters.

Upcoming Educational Events

Calendar

September 2024

Mon

Tue

Wed

Thu

Fri

Sat

Sun

26

27

28

29

30

31

1

2

3

4

5

9:30

🇨🇿 Manufacturer's Post-marketing Activities I – Post-marketing Surveillance (PMS)

+1 more

6

7

8

9

10

11

9:30

🇨🇿 Amendment Regulation on MDR and IVDR

+1 more

12

9:30

🇨🇿 Manufacturer’s Post-marketing Activities II – Clinical Follow-up (PMCF)

+1 more

13

14

15

16

17

18

19

9:30

🇨🇿 Manufacturer's Post-marketing Activities III – Vigilance

+1 more

20

21

22

23

24

25

10:00

🇨🇿 Medical Device Information System – Practical Experience

+1 more

26

0:00

Deadline to Transfer Appropriate Surveillance to a MDR Notified Body for Legacy Devices

+2 more

+3 more

27

28

29

30

1

2

3

4

5

6

Past Events

Thu, 19 Sept
🇨🇿 Manufacturer's Post-marketing Activities III – Vigilance
Online: Cisco Webex
Learn more
19 Sept 2024, 09:30 – 11:00
Online: Cisco Webex
The last in a series of three webinars that will take you through key aspects of post-market monitoring of medical devices, including the PMCF and now the vigilance system. The vigilance seminar is primarily aimed at manufacturers, but this one is also very useful for distributors and importers.
Thu, 12 Sept
🇨🇿 Manufacturer’s Post-marketing Activities II – Clinical Follow-up (PMCF)
Online: Cisco Webex
Learn more
12 Sept 2024, 09:30 – 11:30
Online: Cisco Webex
The second in a series of three webinars that will take you through key aspects of post-market monitoring of medical devices, including post-market clinical follow-up and the vigilance system. This seminar focusing on PMCF of medical devices is primarily aimed at manufacturers.
Wed, 11 Sept
🇨🇿 Amendment Regulation on MDR and IVDR
Online: Cisco Webex
Learn more
11 Sept 2024, 09:30 – 12:00
Online: Cisco Webex
Webinar for manufacturers and importers of medical devices and IVDs, and mainly for hospital representatives. Detailed presentation of a major legislative change resulting in the phased earlier launch of the Eudamed, reporting of MDR/IVD outages and extension of transition periods for legacy IVDs.
Thu, 05 Sept
🇨🇿 Manufacturer's Post-marketing Activities I – Post-marketing Surveillance (PMS)
Online: Cisco Webex
Learn more
05 Sept 2024, 09:30 – 11:30
Online: Cisco Webex
Join us for the first of a series of three webinars that will guide you through the key aspects of post-market surveillance of medical devices. The seminar is primarily intended for manufacturers, but it is also very beneficial for distributors and importers.
Sun, 26 May
Deadline to Lodge an Application for MDR Conformity Assessment for Legacy Devices
Europe
Learn more
26 May 2024, 00:00
Europe
Deadline to lodge an application for MDR conformity assessment for legacy devices that want to benefit from extended transition period.
Sun, 26 May
Deadline to Have MDR QMS in Place for Legacy Devices
Europe
Learn more
26 May 2024, 00:00
Europe
Deadline to have MDR QMS in place (in accordance with Article 10/9 MDR) for legacy devices that want to benefit from extended transition period.
Sun, 26 May
End of Transition Period for Some Legacy Devices
Europe
Learn more
26 May 2024, 00:00
Europe
End of transition period for legacy devices that do not meet the conditions for application of the new transition periods.

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