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OpenClaw Skills & Use Case Index

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Skills with input: Design and manufacturing information

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  • mdr-745-specialist - EU MDR 2017/745 Compliance Specialist for Medical Devices
    EU MDRmedical devicecomplianceregulatory affairs

    ★ 8 · Updated 2026-06-30

    EU MDR 2017/745 compliance specialist for medical device classification, technical documentation, clinical evidence, and post-market surveillance.

    ⚙ Classify medical device under MDR⚙ Prepare technical documentation per Annex II/III⚙ Develop clinical evidence strategy