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Kiwa Medical returns to RAPS Euro Convergence
24 April 2025
Kiwa Medical is back at RAPS Euro Convergence 2025! Meet our experts at Stand 25 in Brussels to explore the latest in MDR certification, regulatory compliance, and clinical investigations. Don’t miss our expert-led sessions on biocompatibility and MDR updates.
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Essential contractual elements for critical suppliers under MDR: A practical guide for manufacturers
22 April 2025
Properly constructed supplier agreements are not just contractual necessities—they are essential risk management tools. By integrating MDR legal requirements with internationally recognized best practices, manufacturers can strengthen their regulatory compliance and product quality, while minimizing business risk
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Effective CAPA Plan Management: Timelines, Root Cause Analysis, and Corrective Actions
14 April 2025
Discover the best practices for effective CAPA (Corrective and Preventive Action) plan management, and the importance of meeting Notified Body timelines, conducting thorough root cause analysis, and distinguishing between corrections and corrective actions.
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Overview of AI-Enabled SaMD and SiMD Devices
20 March 2025
Artificial Intelligence (AI)-based software medical devices are revolutionizing the healthcare sector in diagnosis, treatment, and patient management. AI-powered Software as a Medical Device (SaMD) and Software in a Medical Device (SiMD) applications cover a wide range of solutions, from medical decision support systems to patient monitoring tools.
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Placing medical devices in Great Britain and Northern Ireland: key differences and timelines
18 March 2025
The rules for placing medical devices on the Great Britain (GB) and Northern Ireland (NI) markets differ primarily in terms of the timelines and regulatory frameworks
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Medical device registration in Great Britain and Northern Ireland
17 March 2025
Registration of certain medical devices which are reusable Class I devices, upclassified Class I devices, and/or reliant on expired/expiring CE certificates in Great Britain (GB) and Northern Ireland (NI).
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What are the requirements for registering medical devices with MHRA?
10 March 2025
To register medical devices with the MHRA, manufacturers must follow specific requirements and procedures. In this article you will find the key steps and requirements.
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Importance of and effective Post Market Surveillance (PMS) – The view of the Dutch Competent Authority (IGJ).
26 February 2025
The Health and Youth Care Inspectorate (IGJ) has identified significant deficiencies in post-market surveillance (PMS) among medical device manufacturers in the Netherlands. IGJ urges manufacturers to prioritize PMS, enhance their knowledge, and ensure compliance to improve device safety and performance.
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Navigating the Regulatory Landscape for Drug-Device Combinations: Key Highlights and Compliance Essentials from EMA (European Medicines Agency)
24 February 2025
A new revision of Questions & Answers for applicants, marketing authorization holders of medicinal products and notified bodies with respect to the implementation of the Regulations on medical devices and in vitro diagnostic medical devices (Regulations (EU) 2017/745 and (EU) 2017/746) has been published.
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Enhancing usability in medical devices: A key to MDR compliance and patient safety
20 February 2025
In the ever-evolving field of medical technology, usability engineering has become a critical factor in ensuring patient safety and regulatory compliance. The MDR (Medical Device Regulation) places a strong emphasis on usability engineering. Compliance with IEC 62366-1 and IEC TR 62366-2 is not just a regulatory requirement but also a best practice for designing medical devices that are safe, effective, and user-friendly.
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PRRC vs UKRP: Navigating medical device regulatory responsibilities
17 February 2025
Two key roles in the medical devices sector are the Responsible Person for Regulatory Compliance (PRRC), which is a requirement under the EU MDR (2017/745) and IVDR (2017/746), and the UK Responsible Person (UKRP), which is mandated under the UK MDR 2002 (SI 2002/618, as amended). While their names may sound similar, their responsibilities and legal implications are quite different.
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Understanding OOS and Deviations in the Medical Device Industry
29 January 2025
In the medical device industry, maintaining quality and compliance is paramount to ensure patient safety and product efficacy. Two critical concepts that often arise in this context are Out-of-Specification (OOS) events and Deviations. While both indicate potential quality or compliance concerns, they differ significantly in their focus, triggers, and resolutions.
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Key Considerations for EN IEC 60601-1 Testing
23 January 2025
EN IEC 60601-1, Medical Electrical Equipment – Part 1: General Requirements for Basic Safety and Essential Performance, is a harmonized standard that outlines the essential safety and performance criteria for active medical devices. Incorporating this standard during the design phase of electrical medical devices is crucial.
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What is Clinical Evaluation Equivalence and does that apply to your medical device?
16 January 2025
Are you considering substantiating the clinical data of your device based on an equivalence device? Do you have full access to clinical data for technical, biological and clinically similar devices and you wish to leverage that to prove compliance for another device? This article could help you get a feeling of whether this could be an option.
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Position Paper of Team NB adopted: MDR Certification Process (including Pre-application, Application and Post Application phases)
14 January 2025
The Position Paper “MDR Certification Process (including Pre-application, Application and Post Application phases) – Consensus document” was adopted by the Team NB members and published on December 18th 2024. This Position Paper is applicable to both legacy devices (pursuant to Article 120) transitioning to MDR, and devices that are new to the market and have not been certified under the Directives before and is aligned to the requirements of MDR
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EU: Commission publishes second draft of GPAI (General Purpose Artificial Intelligence) code of practice
6 January 2025
On December 19, 2024, the European Commission published the second draft of the 'General-Purpose AI Code of Practice.' Independent experts present the second draft of the General-Purpose AI Code of Practice, based on the feedback received on the first draft, published on 14 November 2024.
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