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Biomedica Translations is a leading provider of translations for clients in the pharmaceutical and biotech industry for regulatory submissions, manufacturing, marketing and post-marketing surveillance or pharmacovigilance.

Our in-depth knowledge of the product life cycle from chemical manufacturing through clinical trial, market authorization submission, and marketing communications means we are uniquely qualified to support the translation needs of this highly specialized industry.

Pharmaceutical and biotechnology translations expertise

Biomedica Translations has unrivalled experience with drug development, clinical regulatory documentation and translating the following types of documents:

• Patents

• Adverse Event Reports

• Dossiers

• CMSs

• PI and PILs



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