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Technology Scouting – Expert Knowledge. Networking. Good conversations.

On 7 April, the medways technology scouting will take place live on site in Jena – with the BAYOOSOFT Risk Manager. Because the topic of the day is the implementation of the MDR and IVDR with the help of digital tools.

One solution for coping with the MDR/IVDR requirements, especially in the area of documentation, is the automation of processes. Software solutions, such as the BAYOOSOFT Risk Manager, support manufacturers on their way to efficient digitalisation.

The aim of the technology scouting is to highlight potentials and to make the synergies of the network visible and usable.

Registrations are possible until 1 April.

Register now (in german)

What we talk about

Software-supported regulatory affairs processes – the fast track to technical documentation

Companies that manufacture medical devices must not only be innovative in development, but also faster than their industry peers when it comes to market launch. Compliance with the MDR, especially the creation and updating of technical documentation, is the responsibility of the Regulatory Affairs Team.

Whenever several standards have to be complied with, it is necessary to bundle the knowledge of different experts and avoid duplicate data storage. The use of software can support manufacturers in making regulatory affairs processes transparent and uniform throughout the company. Your regulatory affairs team is supported in all phases of product approval and routine work is efficiently mapped – so that your experts can concentrate fully on the content and your time to market is shortened.

Franziska Weiß
https://www.linkedin.com/in/franziska-weiss/

Franziska Weiß

Head of Sales

Together with her team, Franziska Weiß has set herself the goal of supporting, accelerating and ultimately automating processes with high regulatory requirements of medical device manufacturers and in the area of IT security.
Since 2017, she has been working for BAYOOSOFT, a manufacturer of management software made in Germany.

BAYOOSOFT

About BAYOOSOFT Risk Manager

Risk Manager Logo

For 18 years now, the market leader has been supporting medical device manufacturers with a process-oriented approach in the creation of risk management files according to ISO 14971, usability engineering according to IEC 62366, creation of the conformity report according to IEC 60601-1 and fulfilment of the basic requirements of MDD, IVDD, MDR and IVDR.

The efficient way to technical documentation: Get to know the BAYOOSOFT Risk Manager free of charge.

test now for free

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Contacts at BAYOOSOFT 

Svenja Winkler
CEO
[email protected]

 

 

Franziska Weiß
Head of Sales
[email protected]

Darmstadt
Lise-Meitner-Straße 10
64293 Darmstadt

Munich
Aidenbachstraße 54
81379 München

Berlin 
Mariendorfer Damm 1-3
12099 Berlin

Contact: [email protected]
Jobs: [email protected]
Press: [email protected]

Phone: +49 (0) 6151 – 86 18 – 0
Fax: +49 (0) 6151 – 86 18 – 150

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How is the classification of medical devices according to MDR carried out? BAYOOSOFT @DMEA 2022
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