Johner Institut
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Significantly shorten your time to market with our proven processes and readily available resources. No more delays due to regulatory hurdles.
Increase your productivity by focusing on product development and sales. We'll take care of all regulatory compliance.
Save the costs of your own regulatory affairs staff and QM system. Benefit from plannable costs without any expensive surprises.
Stay calm – knowing that your medical devices meet all regulatory requirements and will pass audits with flying colors.
The increasing MDR and ISO 13485 requirements pose major challenges for many manufacturers.
A lack of capacity, expertise, or unsuitable QM systems delay the market launch of their medical devices and jeopardize their business success.
Our legal manufacturer service includes:
Contact us right away to request a first meeting.
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+49 7531 94500 20
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