IFUs Translation

For medical device and diagnostics manufacturers striving to bring their products to the global market, expertly translated IFUs are a critical component of success. You can achieve the best translation results, quickly and cost-effectively, by working with an IFUs translation expert who thoroughly understands the special technical and legal requirements for IFUs translations.

You can count on Merrill Brink International to deliver the professional IFUs translation services you need.

In-depth IFUs translation expertise

Merrill Brink has over 20 years’ experience in the medical device and diagnostics industries. Our medical linguists’ subject matter expertise is second to none. In medical specialties such as audiology, cardiology, endoscopy, neurology, orthopedics, respiratory physiology, urology and vascular surgery, our expert knowledge ensures accuracy and consistency in terminology, reducing the risk of errors and the need for time-consuming edits.

Our medical translation experts have worked on a wide range of materials including:

IFUs/DFUs Product labeling Package inserts Training manuals SmPCs Clinical trial documentation

Clinical study protocols Case study report forms Patient questionnaires Clinical study report forms Patient diaries/ forms/ materials

Informed consent forms Patient report outcomes (PROs) Core data sheets Scientific articles

Your projects are managed by professional, customer service-committed project managers with years of risk management experience.

Unmatched quality assurance and risk analysis

Merrill Brink is one of the few IFUs translation service providers in the world that meets a variety of international quality standards. Our commitment to these rigorous standards means you never need to worry about the safety and security of all of your translation materials.

Merrill Brink has proven experience with international business and regulatory standards such as:

FDA regulatory programs European Union Directives: Medical Device Directive 93/42/EEC (MDD) In Vitro Diagnostic Medical Device Directive 98/79/EEC (IVDD) Active Implantable Medical Device Directive 90/385/EEC (AIMDD)

Active Implantable Medical Device Directive 90/385/EEC (AIMDD) Directive 2004/27/EC concerning human medicines Japanese Pharmaceutical Affairs Law (PAL) ISO quality and risk management standards CE Mark requirements

Proven, reliable IFUs translation services

When you need reliable, responsive IFUs translations services, choose the industry leader – Merrill Brink International.

Contact Merrill Brink today.