Introduzione

Course linked to
MedDev Day Conference  - "MDR 2017/745 Reality Check – Readiness of the EU System"
27 September 2022 - Barcelona


The Periodic Safety Update Report (PSUR) is an entirely new type of report that has been introduced in Article 86 of the Medical Device Regulation (MDR).
It requires manufacturer of class IIa, class IIb and class III devices to prepare a Periodic Safety Update Report (PSUR) for each device and where relevant for each category or group of devices summarizing the results and conclusions of the analyses of the PMS data gathered.

The regulatory requirement is set, yet the PSUR is a new document and manufacturers often do not have a clear view of what it entails:

  • What do MDCG guidelines say?
  • What are the expected data sources that need to be analysed and presented?
  • Which type of preventive and corrective actions need to be listed in the PSUR?
  • What are the main findings that should come out of the PSUR?
  • Where does it fit within the PMS context and other post-market documents such as the PMCF Evaluation Report, the CER and the SSCP?

This workshop will provide relevant information to draft a PSUR, including what data should be presented and how it should be reported. It will offer the experience of an industry-expert for all representatives involved in working with medical devices under the MDR umbrella.

  • The regulation, the guidelines and their context
  • Submission obligations and timelines
  • Data to be presented and how it should be presented
  • Reportable data and main findings
  • Challenges and lessons learned from first experiences

The course is addressed to:

• Clinical Affairs
• Post-Market Surveillance
• Regulatory Affairs
• Medical Writers
• Product Managers
• CROs

Interactive training

Docente/i
Markus Pöttker
Info

Markus Pöttker

PMS EU MDR Workstream Lead at Smith&Nephew
Markus is a member of the EU MDR Project team at Smith&Nephew leading the Post Market Surveillance work stream. In this role, he is responsible that the requirements of the EU MDR are correctly interpreted and implemented across the company. Prior to this, he spent seven years in Quality & Regulatory roles, at last he was the Director of Complaint Management and Head of Regulatory Compliance with global responsibility for Complaint Handling, Medical Device Reporting and interaction with Regulatory Agencies. Markus is co-chair of MedTech Europe’s PMS & Vigilance Working Group and a member of the MDCG Task Forces for Vigilance, PSUR and PMS. Markus holds a master’s degree in law from WWU Münster, Germany. Markus is a bridge builder between the regulatory requirements for medical devices and practical implementation in companies. In addition to complex regulatory issues, he is passionate about digitalisation and lean process optimization - but also about human communication. He believes that technical innovation will continue to transform the medical technology industry.

26 September 2022
from 14:00 to 18:00 – 4 hrs with a coffee-break midway

Training venue:
H10 Marina Barcelona
Av. Bogatell, 64-68 – E08005 – Barcelona

H10 Marina Barcelona is 10 minutes walk from the beach and 5 minutes away you have the Olympic Village. Closer to the Metro stop, Bogatell: it is just 2 minutes behind the hotel and can take you into the city centre in 15 minutes, or you could even walk in about 30-40 minutes.

100 m from Bogatell metro station (Line 4)
300 m from Marina metro station (Line 1)
15 km from Barcelona-El Prat airport

The course will proceed with a minimum number of participants.
Should this number not be reached the registered participants will be notified one week prior to the commencement of the course.

 

Early Bird: € 560,00* (until 29 August 2022)

Ordinary: € 670,00*

Freelance – Academy – Public Administration**: € 310,00*


*for Italian companies: +22% VAT

**Early Bird discount not applicable to Freelance – Academy – Public Administration fee

The fee includes: seat at the training, training material, coffee break, organisational office assistance, certificate of attendance.

Versione Stampabile
Cosa saprai fare dopo il corso
Risultato atteso
Understand the regulatory requirements for PSUR
Risultato atteso
Identify the relevant input documents for your PSUR
Risultato atteso
Prepare PSURs for different device classifications
Risultato atteso
Understand challenges and lessons learned from first experiences of PSUR preparations

<p style="text-align: center;"><strong>H10 Marina Barcelona<br />
</strong><span>Av. Bogatell, 64-68</span><br />
<span>E-08005 – Barcelona</span></p>

H10 Marina Barcelona
Av. Bogatell, 64-68
E-08005 – Barcelona

<p style="text-align: center;"><strong>H10 Marina Barcelona<br />
</strong><span>Av. Bogatell, 64-68</span><br />
<span>E-08005 – Barcelona</span></p>
<p style="text-align: center;"><strong>H10 Marina Barcelona<br />
</strong><span>Av. Bogatell, 64-68</span><br />
<span>E-08005 – Barcelona</span></p>
<p style="text-align: center;"><strong>H10 Marina Barcelona<br />
</strong><span>Av. Bogatell, 64-68</span><br />
<span>E-08005 – Barcelona</span></p>

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