Helping Manufacturers Bring Products to International Markets with Confidence
Medical device content is highly technical, tightly regulated and constantly evolving. Whether you’re launching a new device, updating Instructions for Use or preparing documentation for additional markets, every translation must remain accurate, consistent and appropriate for its intended audience.
ALM works with manufacturers, software providers and healthcare technology companies to create multilingual processes that support the entire product lifecycle, not simply individual translation projects.
We combine specialist medical device linguists with terminology management, translation technology, controlled review and technology-enabled workflows to help reduce multilingual content risk while improving consistency and efficiency over time.
For a translation partner that understands your industry, contact ALM:
Get a Free Quote How compliant is your translation process?Medical Device Content We Translate
From technical documentation and IFUs to software and regulatory
content, we help every part of your multilingual journey.
Instructions for Use (IFUs)
Accurate, user-focused translations that help maintain clarity, consistency and support regulatory requirements across every language
Technical Documentation
Supporting multilingual technical files, product specifications and engineering documentation for international submissions.
Product Labelling & Packaging
Maintain approved terminology and consistent messaging across labels, packaging and product information.
Medical Software
Localisation for software interfaces, digital health platforms, connected devices and Software as a Medical Device (SaMD).
Regulatory Documentation
Translation support for MDR documentation, technical files, submissions and supporting regulatory materials.
Marketing & Training
Create consistent multilingual experiences across websites, product brochures, e-learning and healthcare professional education.

How Compliant is Your Translation Process?
How confident are you that your multilingual documentation would stand up to regulatory scrutiny?
Take our five-minute assessment to benchmark your current translation process, identify potential risks and receive practical recommendations tailored to your organisation.

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