We prepared all the technical documentation ready with Signature on your templates.
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Medical Devices

technical
documentation

In-vitro-Diagnostic

We create/revise your IVD technical documentation quickly and efficiently.
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Medical Device Software:
Our team reliably accompanies you through all phases of the software life cycle of your medical device.
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Medical Devices

Software

In-vitro-Diagnostic

Medical Device Software:
Our team knows the regulatory requirements for IVD software.
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Find out how verification and validation can accelerate the development process of your medical devices.
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Medical Devices

Validation
Verification

In-vitro-Diagnostic

Verification and validation of your IVD: Reduce development costs and time-to-market with Metecon.
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Clinical Affairs: Mastering the challenges of the MDR and other regulations with us.
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Medical Devices

Clinical Affairs

In-vitro-Diagnostic

Clinical Affairs: Mastering the challenges of the IVDR and other regulations with us.
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Regulatory Affairs: Optimization efficient through a strategic approach.
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Medical Devices

Regulatory
Affairs

In-vitro-Diagnostic

Regulatory Affairs for IVD: Our team knows the requirements for international regulatory approval.
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QM-Systems are the basis for the quality and regulatory compliance of your medical devices.
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Medical Devices

Quality
management

In-vitro-Diagnostic

IVD-Quality Management with Metecon: Best prepared for EN ISO 13485:2016.
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