10th of September 2019

6th of September


Zürich, Switzerland 


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MedBraid 2010 is a one day educational and networking event offering to industry expertise on critical topics to success in medical devices manufacturing and to ensure the safety of product for end-user. The seminar offers an opportunity for industry to understand the basics, interpretation, application & being update with recent changes on the standards. The seminar will cover issues related to manufacturing of products, microbiological contamination of product, clinical trial & sterilization.



The presentations taking place at MedBraid 2010 will be: 

  • Clinical evaluations and clinical trials for medical devices

  • EN ISO 11607(2006): Packaging for terminally sterilised medical devices

  • Microbiological Monitoring of Medical Devices and Clean Rooms – Importance and Approaches based on ISO 11737-1 and ISO 14698-1/-2 respectively

  • EN ISO 11607(2006) : Packaging for terminally sterilised medical devices

  • Water used in Medical Devices Manufacturing – European and US pharmacopeias”

  • “Method for prediction of ethylene oxide lethality and cycle development”

  • “Directive 2007/47 EC - Successful implementation of the key revisions to the medical device directives”

  • “US-FDA 510(k) submissions- Requirements and their practical implementation”

  • “Software Development Lifecycle (IEC 62304)”

Please click here to learn more about our experts and chairman.

Please click here to get access to the MedBraid 2010 official Schedule. 


MedBraid 2010 is brought to you thanks to: