Medical Instruments And Equipment Translation
Expert medical instruments and equipment translations by an industry leader
To succeed in today’s global marketplace, medical instrument and equipment companies need an expert language partner who can help them quickly and accurately communicate in multiple languages. Equally important, you need a partner who understands the precision, adherence to deadlines and risk management requirements inherent in medical instruments and equipment translations.
That’s why so many companies rely on Merrill Brink International. Our quality-driven and rapid translation turnaround times can help streamline the process. We can also ensure that your global marketing campaign is delivered on time, in an accurate and culturally sensitive way.
In-depth medical instruments and equipment translation expertise
Merrill Brink has over 30 years’ experience in providing medical instruments and equipment translations. Our medical linguists’ subject matter expertise is second to none. Our medical instruments and equipment translation experts have worked on a wide range of materials including:
| • Equipment manuals | • Product labeling | • Newsletters |
| • Software instructions | • Package inserts | • Brochures |
| • Product specifications | • Training manuals | • Presentations |
| • Regulatory documents | • Safety manuals | • eLearning |
| • Installation guides | • Core data sheets | • Web sites |
Unmatched quality assurance and risk analysis
Merrill Brink is one of the few medical instrument and equipment 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: |
| • Japanese Pharmaceutical Affairs Law (PAL) | o Medical Device Directive 93/42/EEC (MDD) |
| • ISO quality and risk management standards | o In Vitro Diagnostic Medical Device Directive 98/79/EEC (IVDD) |
| • CE Mark requirements | o Active Implantable Medical Device Directive 90/385/EEC (AIMDD) |
| o Directive 2004/27/EC concerning human medicines |
Proven, reliable medical instrument and equipment translation services
When you need a medical instrument and equipment translations service provider with proven experience, choose an industry leader – choose Merrill Brink International.