May 2024 News Letter

Great news everyone! Patient Guard is thrilled to bring you fresh updates through our May 2024 newsletter. We’re super excited to share that we’ve started offering Training courses – kicking off with our inaugural course on ‘EU Medical Device Regulations 2017/745’.
May 2024 News letter from patient guard for all the latest medical device and IVD regulatory and quality assurance news.

Patient Guard News

We’re planning to conduct these insightful sessions once every month, accommodating up to 4 participants per course. The best part? It’s all happening virtually via Microsoft Teams, guided by our expert Patient Guard trainer. So, if you or your colleagues are eager to deepen your understanding of EU regulations, this is your perfect opportunity. To find out more click below

Regulatory News

European Union

Here we show medical device and IVD news and updated MDCG documents issued by the EU for the month of April 2024.

EU Commission News

  • A Study and dashboard on reprocessing and reuse of single-use-devices in the EU
  • MDCG 2024-4 – Safety reporting in performance studies of in vitro diagnostic medical devices under Regulation (EU) 2017/746 – April 2024
  • Update – MDCG 2022-9 rev.1 – Summary of safety and performance template – April 2024
  • MDCG 2024-5 – Guidance on the Investigator’s Brochure content – April 2024
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United Kingdom

Here we show medical device and IVD news shared by the MHRA in the month of April 2024.

MHRA News

Impact of AI on the regulation of medical products

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United States

Here we show medical device and IVD news shared by the FDA in the month of April 2024.

FDA News

  • CDRH 2024 Innovation Report (April 2024)
  • CDRH 2024 Safety Report (April 2024)
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Patient Guard News

Here we show all the latest medical device and IVD standards that have been issued by BSI in the month of April 2024.

  • BS EN 17854:2024 – Antimicrobial wound dressings. Requirements and test method

  • BS ISO 5832-4:2024 – TC – Implants for surgery. Metallic materials – Cobalt-chromium-molybdenum casting alloy

  • BS EN ISO 5832-1:2024 – TC – Implants for surgery. Metallic materials – Wrought stainless steel

  • BS EN ISO 5832-7:2024 – Implants for surgery. Metallic materials – Forgeable and cold-formed cobalt-chromium-nickel-molybdenum-iron alloy

  • BS EN ISO 8637-2:2024 – TC – Extracorporeal systems for blood purification – Extracorporeal blood and fluid circuits for haemodialysers, haemodiafilters, haemofilters and haemoconcentrators

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Medical Device Consultancy Companies

A medical device consultancy is a firm that offers specialized services for companies involved in the development, manufacturing, and marketing of medical devices. These consultancies typically have teams of experts who provide a wide range of services, from regulatory strategy to product development, quality management systems (QMS), and market access.

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In Vitro Skin Irritation Testing: ISO 10993-23 Standard

Skin irritation occurs when a substance causes inflammation or damage to the skin upon contact. For medical devices, this can be a serious concern, as they are often in prolonged contact with the skin. The consequences of not adequately testing for irritation can range from minor redness to severe dermatitis, leading to discomfort, injury, or even infection in users. Therefore, reliable testing methods are crucial to ensure that products are safe before they reach the market.

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Cytotoxicity Testing in Medical Device Biological Evaluation

In the highly regulated world of medical devices, ensuring patient safety is paramount. One of the essential components of this safety assurance is cytotoxicity testing, specifically adhering to ISO 10993-5 standards. This blog explores the importance of ISO 10993-5 cytotoxicity testing, particularly for medical devices that come into direct contact with patients, and how it contributes to the overall safety and efficacy of these devices.

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Drug Stability in Medical Devices: Syringes, Infusion Sets and Bags

Ensuring the stability of drugs in contact with medical devices such as syringes, infusion administration sets and infusion administration bags is paramount. This article delves into the importance of drug stability testing, the challenges faced, and the methodologies employed to guarantee that the drugs administered through these devices remain safe and effective.

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