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CE marking — Medical devices (Regulation MDR 2017/745)
A medical device without CE marking under MDR Regulation 2017/745 remains strictly prohibited from marketing in the European Union.
TargetUp Consulting — Morocco & AfricaPresentation
We manage your compliance: classification of the device, implementing the ISO 13485 quality management system, technical dossier and documentation, risk management (ISO 14971), clinical evaluation, and supporting the notified body through to the certification audit and CE marking.
Why TargetUp: triple expertise in Consulting + Financing + Training under one roof, team of senior consultants, rooted in Morocco & French-speaking Africa.
👉 Request a quote or consultation: book your 360° flash diagnosis, with no obligation.
Support provided by senior consultants
Executives, quality managers, R&D and operators subject to normative requirements or market access
A recognised consulting partner
Sectoral Expertise
Senior consultants who understand your business and your standards.
Anchoring Morocco & Africa
A thorough understanding of the local regulatory and economic context.
Contractual commitment
A reinforced obligation of means, marked and contractualised.
Proven method
A structured Lean approach: frame, measure, improve, sustain.
Skills transfer
Your teams become autonomous in the process.
Accreditation Network
A recognised ecosystem of certifications and affiliations.
You may be wondering…
What is the cost of this support?
Do you operate throughout Africa?
How do you get started?
Request your quote
Fill out this form: a TargetUp consultant will contact you with a tailored proposal.
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