With our experience in Europe, North and South America, Asia and the Middle East we can help you to a rapid market approval in all regions. Whether for short or long term contracts – we can manage your product registrations for all target markets, supported by our in-house software REGULA™. We offer long-term experience in writing clinical evaluation reports.
«We had a workshop about the regular strategy for our MedTech startup and were very happy with how Mr. Riedwyl handled the session. It was a very open, highly interesting and informative dialogue, giving us precious insights and helping us to set up our regulatory strategy to reach certification. The know-how of ISS with the open attitude of the team, listening to us as customers, was perfect ...»
ISS-Talk at the Tuttlinger Innovationsforum on October 19th
02 August 2017
Digital Regulatories is a hot topic....
3D Printing, impact of MDR
25 June 2017
ISS CEO Hansjörg Riedwyl is a...
Formation – Évaluation clinique selon MEDDEV 2.7/1, Révision 4
02 March 2017
ARIAQ et ISS AG proposent une...
MDR event with participation of ISS
09 February 2017
At the first Swiss Medtech Conference...
Further clinical evaluation of ISS AG meets the requirements
26 January 2017
The process established by ISS AG...
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