Introduzione
Post-Market Clinical Follow-up (PMCF) as part of Post-Market Surveillance is not a new requirement under the MDR. But requirements on how and when to do PMCF and on how to document these activities have been enforced. Each device (or device family) needs a specific PMCF Plan and results of PMCF activities are summarized in a PMCF Evaluation Report.
These documents are subjects to predefined review cycles and depend on several other input documents. The collection of clinical data is often time-consuming and expensive. The PMCF Plan aims to organise well-considered PMCF activities to generate the missing data. To be able to work on your PMCF Plans, you need to know general and specific methods for PMCF, the input documents and the trigger for PMCF. The results presented in the PMCF Evaluation Report will also affect several other parts of the Technical Documentation.
This course will give you profound insights into the regulatory requirements for PMCF, best practice advice on how to prepare PMCF Plans and Reports, as well as insights in common pitfalls and tips on how to prevent them.
Module 1
- Introduction to Annex XIV Part B of EU MDR 2017/745 (Post-Market Clinical Follow-up)
- Structure and Content: The MDCG (Medical Devices Coordination Group) Guidance on PMCF Plans (2020/7)
- Input documents and review cycles
- General and specific methods for PMCF
Module 2
- Structure and Content: The MDCG (Medical Devices Coordination Group) Guidance on PMCF Evaluation Reports (2020/8)
- Practice with a fictional medical device
- Common pitfalls and strategies to avoid them
Medical writers, Clinical Affairs, Quality Assurance, Product Managers.
Attendees’ experience
This course is intended for personnel with little or no experience in regulatory writing, including PMCF Plans and PMCF Evaluation Reports, under the Medical Devices Regulation 2017/745 (EU MDR).
The workshop will be a mixture of presentations, team discussion, brainstorming and practical examples.
Docente/i
Katharina Friedrich
Katharina Friedrich is a medical writer with experience in MDR regulatory writing. She is based in Heidelberg, Germany and works as a Freelance Medical Writing Consultant with focus on orthopedic and cardiovascular devices. She prepares Clinical Evaluation Plans and Reports, PMCF Plans and Reports and SSCPs in compliance with MDR 2017/745 for class I to class III devices. She also supports development projects and the conduction of PMCF activities. As medical doctor she has experience in the field of orthopedic and trauma surgery.
Online training – 2 modules
MODULE 1 | 26 April 2023 09:00 am – 12:45 pm CEST
MODULE 2 | 28 April 2023 09:00 am – 12:45 pm CEST
After the registration, you will receive all details about the connection.
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: € 825,00* until 14/04/2023
Ordinary: € 945,00*
Freelance – Academy – Public Administration**: € 536,00*
*for Italian companies: +22% VAT
**Early Bird discount not applicable to Freelance – Academy – Public Administration fee
The fee includes: tuitions, organizational office assistance, teaching materials and attendance certificate that will be sent after the training via e-mail.
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Online interactive training on Zoom platform.
LS Academy will provide the access link to the virtual platform a few days before the training.