Professional translation in the area of medicine and pharmacy

Our highly skilled translators and revisers of medical documentation, support the efforts of pharmaceutical companies and medical establishments to reach their Bulgarian clients and comply with stringent legal requirements for doing business in this heavily regulated area.

If you require translation of drug marketing applications, drug dosage and use instructions, short product descriptions, leaflets, package inscriptions, product brochures, drug trial documentation, informed consent forms, drug safety sheets, declarations of conformity for medical devices, history of disease records etc., INTERLANG is fully equipped to handle your project and deliver it within the strictest deadline and in strict compliance with quality requirements.

INTERLANG is one of the leading providers of translation services to medical and pharmaceutical companies and public and private healthcare establishments.

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We have translated for:

  • The Ministry of Health
  • The National Health Insurance Fund
  • The International Healthcare and Health Insurance Institute
  • The Translation Centre for the Bodies of the European Union (CDT)
  • Solvay Pharmaceuticals
  • GlaxoSmithKline
  • Merck
  • Servier Medical EOOD
  • Schering AG
  • Johnson & Johnson
  • AmGen Bulgaria
  • DutchMed  
  • BBraun Medical SA
  • Convex
  • The Association of Pharmacists in Bulgaria etc.

Specialist terminological databases in medicine and pharmacy

All our translators have access to general and specialist dictionaries, glossaries and terminology tools which guarantee translation precision, terminological accuracy and consistency.

INTERLANG maintains and regularly updates its database, which includes the latest available European Pharmacopoeia, the Standard terms of medicines and drugs, packages and routes of drug administration. We monitor changes in the document templates, basic and specialist terms, approved by the European Medicines Agency (EMA) and the Bulgarian Executive Agency for Drugs relevant to centralised or national procedures for evaluation, marketing authorisation and registration of drugs and medicinal products, types of drugs (used in human and veterinary medicine) and medical devices.

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Our clients rely on us for the translation of:

  • Clinical trial protocols
  • Terms of reference
  • Dossiers
  • Medical product registration documentation
  • E-training materials
  • Hospital discharge summary
  • Drug safety notices
  • Drug dosage and application instructions
  • Informed consent forms
  • Declarations of conformity for medical devices
  • Instructions for the use of medical devices
  • Packaging inscriptions and leaflets
  • Patient logs
  • Patient information
  • Patient questionnaires
  • Patient result reports
  • Preclinical and clinical trials
  • Clinical trial contracts
  • Reports
  • Short product descriptions
  • Toxicology test reports
  • Training materials
  • Synopses
  • Tests for the certification of administrative personnel in the area of clinical trials
  • Patents
  • Drug use applications
  • Product certificates

Contact us today by completing our online  enquiry/order form, by e-mail or by phone on +359 2 808171. It will be our pleasure to give you a quote that is customised to any specific requirements you may have.

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