Life science, Pharmaceutical, Medical and Biotechnology

 
 
national-cancer-institute-byGTytEGjBo-unsplash.jpg

Global Languages and Cultures, Inc. provides high quality translations for the CRO, pharmaceutical and biotech industries. Our estimates for language services are firm allowing you to stay within your budget. GLC translators are native-speaking linguists with many years of experience in the medical, pharmaceutical and CRO fields, providing accurate, fully-formatted document translations that are faithful to their originals. In order to comply with regulatory requirements we can also provide back-translations and certifications upon request. Our exclusive retainer agreements with the world's top medical translation experts allow us to provide you with top quality translations at a reasonable cost compared to our competitors. Additionally, thanks to our efficient project management system we will easily meet or beat your deadline requirements. Click on the links above to read more about our experience in these fields.

List of Services

  • Back Translations

  • Case Report Forms (CRF)

  • CE Mark Compliance Translations

  • Clinical Protocols

  • Clinical Trials

  • Comprehensive Medical Research Studies

  • Consent Form Translationss

  • Data Sheets

  • Dossiers

  • Drug Registration Documentation

  • ICF Translations

  • INDs

  • Industrial, Technical and Sales Training Manuals

  • International Regulatory Submissions

  • Interpreters for Meetings

  • IVR - Interactive Voice Response

  • Label and Package Inserts

  • Manuals

  • Manufacturing Process Description

  • Medical Translations

  • Medical Device Manuals

  • NDAs

  • Package Inserts and Labels

  • Patents and Other Legal Documents

  • Patient Information

  • Patient Questionnaires

  • Pharmacological Studies

  • Pharmaceutical Translations

  • PMAs

  • Product Labels

  • Protocols

  • Regulatory Documents

  • Scientific Papers

  • Toxicology Reports

  • Translations to Comply with EU’s IVDD Directive

  • Voice Prompts

  • Marketing and Advertising Materials

  • Packaging Inserts and Labels for Dental Alloys and Instruments

  • User and Instruction Manuals

  • All Other Technical and Business Documents

  • Interpreters for Meetings Around the World

Success Stories

The meeting planners of the XVth International Aids Conference relied on Global Languages and Cultures Inc. (GLC) for HIV/AIDS related medical translations. The languages included Papiemento, French and Dutch. GLC is proud to be a part of the worldwide HIV/AIDS prevention and treatment efforts.

A pharmaceutical conference in Athens went very smoothly, partly thanks to GLC’s interpreters who provided simultaneous interpretation services to the non-English speaking conference attendees.

A Fortune 50 medical device manufacturer enjoyed great success around the world with its radiology related software translated, localized and tested by GLC into 12 languages.

A medical professionals’ association communicates better with their non-English speaking visitors to their web site, translated into Spanish by GLC.

A leader in the pharmaceutical and genetic engineering fields always makes sure that GLC translates and back-translates all its ICFs, consent forms and protocols into different languages before it starts clinical trials on possible new drug treatments.

Only GLC dental translation experts could have delivered this translation project to our client’s satisfaction. Armed with degrees in dentistry and many years of experience, GLC translators translated alloy inserts into 15 languages for a prestigious dental products company. Whether it is tooth-whitening products or dental instruments, GLC’s expertise in dental translations allow its customers to communicate more efficiently with their target audiences around the world.

IVDD and MDD Compliance

As of December 7th, 2003 all  in vitro diagnostic medical devices  (IVD) sold within the European Union must carry the CE Marking.  The CE Mark is a "certificate" indicating that the device is compliant with all rules and regulations. This directive also includes local language requirements. Additionally, MDD (Medical Device Directive) that was adopted on January 1, 1995 has similar mandates for general medical device manufacturers.

Failure to comply with IVDD or MDD and sell products in the European Union without a CE mark may have significant ramifications.  The manufacturers of such products may face criminal charges as regulatory authorities pull their devices off the shelves.

GLC's experienced medical translation and project team can help you meet IVDD and MDD compliances and sell your products confidently with a CE Mark affixed on them.  Advantages of partnering with us for your language translation needs include:

  • Expert certified medical translators in all languages

  • QA process to deliver flawless translations

  • Experienced project managers to answer all your questions

  • FREE glossary compiling

  • Liaison with your reviewers

  • Timely delivery to meet your deadline requirements

  • Discounted rates to meet your budgets

  • FREE certification of translation