{"version":"https://jsonfeed.org/version/1","title":"Ayewa Consultancy","home_page_url":"https://ayewaconsultancy.com","description":"Ayewa Consultancy","author":{"name":"Ayewa Consultancy"},"items":[{"id":"https://ayewaconsultancy.com/insights/f/medical-device-manufacturing-feasibility-to-commercialisation","html_content":"<img src=\"https://img1.wsimg.com/isteam/stock/yr4xl5p\"/><p>The Strategic Imperative of the Scope of Work</p>","url":"https://ayewaconsultancy.com/insights/f/medical-device-manufacturing-feasibility-to-commercialisation","title":"Medical Device Manufacturing: Feasibility to Commercialisation","summary":"The Strategic Imperative of the Scope of Work","date_modified":"2026-04-20T16:45:52Z"},{"id":"https://ayewaconsultancy.com/insights/f/how-early-polymer-choice-accelerates-medtech-market-access","html_content":"<img src=\"https://img1.wsimg.com/isteam/stock/wNYW6mP\"/><p>In early-stage medical device development, knowing that you need a medical-grade polymer is the easy part. However, identifying the right material on paper and actually structuring a supply chain to support it are two en...</p>","url":"https://ayewaconsultancy.com/insights/f/how-early-polymer-choice-accelerates-medtech-market-access","title":"How Early Polymer Choice Accelerates MedTech Market Access","summary":"In early-stage medical device development, knowing that you need a medical-grade polymer is the easy part. However, identifying the right material on paper and actually structuring a supply chain to support it are two en...","date_modified":"2026-04-07T19:33:20Z"},{"id":"https://ayewaconsultancy.com/insights/f/navigating-euuk-mdr-for-medical-device-companies","html_content":"<img src=\"https://img1.wsimg.com/isteam/stock/2390\"/><p>The EU Medical Device Regulation (EU MDR 2017/745) and the UK Medical Devices Regulations (UK MDR 2002, as amended) have significantly changed the landscape for medical device development.</p>","url":"https://ayewaconsultancy.com/insights/f/navigating-euuk-mdr-for-medical-device-companies","title":"Navigating EU&UK MDR for Medical Device Companies","summary":"The EU Medical Device Regulation (EU MDR 2017/745) and the UK Medical Devices Regulations (UK MDR 2002, as amended) have significantly changed the landscape for medical device development.","date_modified":"2026-02-27T10:04:00Z"}]}