Public seminars and courses

Symbioteq provides trainings in regulatory affairs and quality assurance for people in the medical device industry. All our trainings are organized in cooperation with our partner, Key2Compliance, who also offers corresponding training for the pharmaceutical industry; read more about their training program here:

Upcoming trainings and events

The new European Regulatory Landscape – MDR and IVDR

January 18, DGI.byen, Copenhagen

Key2Compliance AB and Symbioteq Kvalitet AB invites you to a 1-day conference on the new MDR and IVDR. The new regulation will ensure that medical devices and in vitro diagnostic medical devices remain safe while allowing people access to new and innovative treatments. For the industry, this change impacts the process and requirements for placing devices on the market, including changes in device classification as well as new requirements for postmarket activities. This and more will be dealt with during this intense one-day conference.

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QA/RA Leader Medical Devices. Unique training to become qualified QA-RA Leader

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Medical Device Quality Management Systems (QMS) 
— Key requirements in MDR, QSReg and ISO13485

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Auditor/Lead Auditor; Pharmaceuticals and Medical Devices

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In-house training courses

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