Pharmaceutical Translation

Neoplus Translation is providing pharmaceutical translation services to drug companies that want to grow pharmaceutical sales internationally and extend sales across the member states of the European Union (EU). Our quality policy is compliant with the ISO 9001:2015 standard, which was developed especially for translation services providers.

Bringing a new drug to market is a lengthy and expensive process. Pharmaceutical companies can spend up to 10 years and more, and over $500 million to get a new drug to market. Since more and more clinical research and drug manufacturing is being done in multiple countries and in multiple languages, quality language services can help bring a drug to market faster and can help streamline the clinical trial process. Translation may be required at many stages, including clinical research, regulatory submission and review, production and marketing.

Our Pharmaceutical Services:

  • Patient Information
  • Pharmacological Studies
  • Toxicology Reports
  • Clinical Protocols
  • Scientific Papers
  • Product Labels
  • Package Inserts and Labels
  • Drug Registration and Documentation
  • Clinical Trials
  • Summary of Product Characteristics
  • Product Information Leaflets
  • Patent
  • Validation Reports
  • Validation Protocols
  • Dossiers
  • Medical Regulations
  • Manufacturing Process Description