Author name: Snehal

Intraocular Lens Manufacturing

Intraocular Lens (IOL) Manufacturing Consultant in the UK

Medical device Manufacturing /

Intraocular Lens (IOL) Manufacturing Consultant: An Overview Unlock Regulatory-Compliant Intraocular Lens Manufacturing Solutions for the UK and Global Markets Intraocular lenses (IOLs) are transformative medical devices used to replace the eye’s natural lens, most commonly after cataract surgery. As the aging population increases across the UK and globally, so does the demand for high-quality, biocompatible […]

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MRI Machine Manufacturing

MRI Machine Manufacturing in the UK: A Complete Guide to Process, Compliance & Opportunities

Medical device Manufacturing /

What is an MRI Machine? An MRI (Magnetic Resonance Imaging) machine is a non-invasive diagnostic tool that uses strong magnetic fields and radio waves to generate detailed 3D images of the body’s internal structures. Unlike X-rays or CT scans, MRI does not use ionising radiation, making it safer for repeated scans and soft-tissue imaging. Widely

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UK Medical Device Classification

UK Medical Device Classification

UKCA /

UK Medical Device Classification Navigating the UK’s medical device regulatory landscape can be overwhelming, especially following the UK’s departure from the EU. In this article, we’re breaking down the UK Medical Device Regulations 2002 (UK MDR 2002)—from classification basics to conformity assessment—so that manufacturers, distributors, and healthcare professionals can better understand their compliance obligations. What

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MHRA IVD Registration

MHRA IVD Registration: A Complete Guide to Registering Medical Devices and IVDs in the UK

Regulatory Compliance /

MHRA IVD Registration: An Overview Before placing medical devices or in-vitro diagnostic (IVD) devices on the market in Great Britain, manufacturers must comply with the MHRA IVD registration requirements. Governed by the UK Medical Devices Regulations 2002 (UK MDR 2002), this registration ensures that all medical devices and IVDs meet essential safety and performance standards.

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MHRA Medical Device Registration

The Ultimate Guide to MHRA Medical Device Registration

Regulatory Compliance /

Are you planning to launch your medical device in the UK? Understanding the MHRA medical device registration process is crucial for smooth market entry. In this guide, we’ll break down the registration process, costs, timelines, and key requirements to help you achieve compliance effortlessly. What is MHRA Medical Device Registration? MHRA registration is a legal

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