TOP TRANSLATORS WITH MEDICAL EXPERTISE

All Novalins translators are qualified to an MsC, PhD or MD level and have at least 6 years of professional experience translating medical documents.

ENSURED SECURITY AND CONFIDENTIALITY

Your sensitive and confidential documents are safe with us. We use secure file systems, and all of our translators work under a binding NDA.

REGULATORY APPROVAL GUARANTEE

We guarantee our translations will be accurate and follow target health authority (e.g. FDA, EMA, PMDA, CFDA) guidelines, or we'll update them free of charge.

Novalins is a clinical research translation specialist dedicated to deliver the highest standards in linguistic products to clients worldwide, while always being on-time and within budget.

Our years of experience in the clinical trials field enables us to provide industry-standard expertise and to adapt our processes according to the specific needs of each document at every stage of the product development and registration process:

  • Preclinical studies;
  • Phases 0 to IV;
  • Surveys & Drug testing;
  • Dossiers for regulatory approval.

In addition to clinical research translations, Novalins also provides additional language solutions such as the translation and linguistic validation of Patient Reported Outcomes (PRO) instruments, comparative reviews and clinical trial back-translation.

Novalins has a strong and growing team of medical translators and editors who specialise in clinical translation in 120 different languages. All our experts meet a minimum criteria:

  • Native speakers of the target language with perfect command of the source language
  • Extensive linguistic, scientific and medical background (M.A., M.S., PhD, MD)
  • Certified medical translators by recognised bodies
  • Clinical trial & research subject-matter-experts

Novalins offers our clients full transparency on the experience and qualifications of the medical translators and editors who work on their projects.

Novalins offers comprehensive clinical translation and localisation services that cover all documents that are produced at all stages of clinical trials. The most frequently translated documents include:

  • Patient Information Sheet (PIS)
  • Informed Consent Forms (ICFs)
  • Case Report Forms (CRFs)
  • Patient Reported Outcomes (PROs)
  • Patient Questionnaires
  • Study Protocols
  • Patient Diaries
  • Medical Records
  • Investigator’s Brochures

In addition to clinical translation and localisation services, Novalins also offers the following services:

  • QA/QC solutions: Back translation, Source & target text editing by SMEs
  • Linguistic validation of PROs
  • Medical writing
  • Medical translation
  • Medical transcription
  • Data entry (CRFs)
  • Linguistic consultancy
  • Sworn – Certified translation
  • Translation memory management
  • Terminology database management
  • Page formatting (DTP) and layout preparation

Please contact us for the complete list of solutions we offer.

Novalins understand the sensitivity of clinical trials and research documents and all our medical translators and experts work under binding non-disclosure agreements. We are also open to any additional confidentiality arrangements requested by our clients.

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