MedTech Projects Ltd

MedTech Projects Ltd provide regulatory and quality support throughout the medical device/IVD life cyle and have experience in the EU, UK and US regulatory regimes. 𝗦𝗘𝗥𝗩𝗜𝗖𝗘𝗦 We can create, update or simply assist you with your: Regulatory Strategy Quality Management System Requirements Checklist (e.g. GSPR Checklist) Risk Management File Clinical Evaluation Labelling (text and symbol requirements only) UDI Post-market Surveillance Technical File Regulatory Submission/Self-Certification Process We can also act as your: UKRP We are a friendly, dedicated team who are happy to help with any enquiries you have in relation to any support you may need. 𝐂𝐎𝐍𝐓𝐀𝐂𝐓 𝐃𝐄𝐓𝐀𝐈𝐋𝐒 +𝟒𝟒 (𝟎)𝟏𝟒𝟖𝟒 𝟐𝟒𝟔𝟑𝟕𝟑 𝓲𝓷𝓯𝓸@𝓶𝓮𝓭𝓽𝓮𝓬𝓱𝓹𝓻𝓸𝓳𝓮𝓬𝓽𝓼.𝓬𝓸.𝓾𝓴

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