News

New cleanroom area before installation of new production equipment
The production of disposable medical products requires a state-of-the-art manufacturing environment. A critical component of this manufacturing environment is the cleanrooms that provide the required cleanliness.
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No matter in which field, being first is never easy! Especially not when it comes to registering medical devices under the high standards of the new "Medical Devices Regulation" (MDR)! However, the sfm team has tackled this challenge  and solved this demanding task together.

Our customers can now…

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1st – 2nd February | Paris Expo, Porte de Versailles | Paris
Booth C50 in Hall 7.2

Are you looking for the best method to reconstitute lyophilized pharmaceuticals? Then visit us at our booth and let us convince you of our nextaro family.

nextaro - for better solutions

If instead you need an…

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sfm medical devices GmbH started dealing with the requirements of the MDR at a very early stage. This substantial challenge was broken down into several smaller projects and tackled accordingly. The hard work and the effort invested has now paid off and we are proud to announce that sfm is n ow…

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After the successful certification of sfm medicel devices GmbH, at the headquarters of the sfm group in Wächtersbach, the subsidiary safemed medical devices s.r.o. in Prague, has now also been successfully certified according to the ISO 14001 standard. The audit was executed by DQS and proves the…

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