🇨🇿 Quality agreements: Practical tips for manufacturers, importers, and distributors of MDs and IVDs
Few companies can boast that they perform all activities related to the life cycles of medical devices and in vitro diagnostic medical devices internally. In our webinar, we will look at how to set up these activities through other parties correctly so that they are not just a formal burden.


Date
25 Mar 2026, 09:30 – 12:00
Online: Cisco Webex
About
The event is held in Czech language only!
Quality agreement (QA) is one of the most important pillars of the quality management system. It is a prerequisite for compliance with MDR / IVDR and a critical factor for obtaining EU certification, as notified bodies insist on the existence of precise QAs. However, drafting a QA that satisfies all parties, covers the minimum requirements, and is successfully concluded in the form of a signed QA is a major challenge.
This webinar is designed to cover a range of needs, from novice specialists who need to familiarize themselves with the basic parameters of quality agreements to experienced quality professionals who want to deepen their knowledge and optimize contractual relationships with business partners. The aim of the webinar is to provide participants with a comprehensive overview of the preparation and conclusion of QAs. The webinar reflects both the basic requirements of legal regulations and standards, as well as real-world experience.
Who the webinar is for:
Regulatory specialists of manufacturers, importers, and distributors of MDs and IVDs
Quality management department employees
Purchasing department employees
Sales / marketing / customer relations department employees
Legal department employees
Quality management system auditors
Persons in the role of PRRC
Auditors from the ranks of notified bodies
Anyone who works in the field of medical devices and wants to broaden their horizons on this issue
Lecturers:
Mgr. Aneta Dostálová
Ing. Petr Votava
Content:
What is QA, its benefits for manufacturers, importers, and distributors
QA from the perspective of legislation, standards, and recommended documents
Content requirements for supplier QA
Content requirements for distribution QA
Practical tips for concluding QA
Additional information:
During the webinar, participants will have the opportunity to ask questions
Each participant will receive a certificate of participation
A PDF presentation will be sent to all participants
Participation fee:
3.900 CZK excluding VAT
100% cancellation fee applies after bindingly confirmed registration, but with the possibility of sending a replacement participant
Webinar hosted by:
Porta Medica s.r.o.
ID: 03301931, VAT: CZ03301931
Registered office: Opletalova 1525/39, 110 00, Prague 1 - Nové Město