Document Types
- Clinical Research Agreements
- Scientific Articles
- Certificates of Pharmaceutical Product (CPP)
- Legalized Documentation
- Common Technical Documents (CTD)
- Chemistry, Manufacturing, and Controls
- Stability Studies
- Bioequivalence Studies
- Methods of Analysis
- Pharmacokinetic Drug Interactions
- Toxicology Studies
- Data Sheets
- Informed Consent Forms (ICF)
- Case Report Forms (CRF)
- Material Safety Data Sheets (MSDS)
- Suspected Unexpected Serious Adverse Reaction (SUSAR) Reports
- Periodic Safety Update Reports (PSUR)
- Investigator’s Brochures (IB)
- Drug Monographs
- Package Inserts
- Clinical Trial Protocols
- Summary of Product Characteristics (SmPC)

Design

Voice-over, Dubbing and Subtitling
Dubbing
Language Combinations
Why Us
Our Team
We have a robust, professional and highly committed team to satisfy the needs of our clients.
Project Manager: Accompanies clients and manages every stage of their project, offering a timely and personalized service, with a 24/7 availability.
Designer: Designs and maintains the format of the material, achieving a faithful copy of the original.
Translator: Health professional experts who transfer from one language to another the contents of the material, based on its communicative purpose, the target audience, and contextual framework.
Proofreader and Editor: Ensures the faithfulness and flow of the translation at the level of terminology, syntax, semantics, and structure.
Quality Control: Ensures the highest quality of the product, by training and guiding the team, enabling the use of tools, developing strategies of continuous improvement, and strengthening client communication.

Quality Assurance
