Pharmaceutical / Biotech

Pharmaceutical and biotech organizations rely on Burg to translate millions of words per year. Because these highly regulated firms require quality and impeccable diligence for translated documents, our ISO 9001:2008, EN 15038:2006 and ISO 13485:2003 certified (Certification due: Fall 2011) procedures ensure that translations are checked for accuracy and remain consistent at each step. We supply translations to the following departments of our nation’s largest pharmaceutical and biotech institutions:

• Regulatory Affairs & Compliance
• Clinical Trials
• Global Labeling and Packaging
• R & D
• Clinical Operations
• Pharmacovigilance
• Dossier / File Management
• Marketing
• Legal

Typical projects for these departments are as follows:

• Clinical Trial Documentation
• Product Information
• E-learning
• Articles & Journals
• Linguistic Validation
• PROs / ePROs / eCRFs
• QOL Questionnaires
• Websites & Software
• Drug Registration Documentation
• MSDS Conversions
• IVRS / IWRS

Find out more about our services.