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The Translation Gate works with you to deliver professional, and high-quality multilingual translation services for your Pharmaceutical content.
When it comes to the pharmaceutical translation industry, accuracy is a must. Unlike any other industry, any translation mistake could lead to injury or death.
That’s why only medical and pharmaceutical experts and translators must work on any pharmaceutical document that needs to be translated. Following the most up-to-date technology in the pharmaceutical field, the translation must be done accurately with the highest level of quality check and ensure that there are no errors available, especially when we talk about the regulations on new drug development and marketing in the United States, the European Union, China, and Japan.
In the first place, comes the drug trials and patents. A very large portion of the clinical research is done in many different countries and runs into many trials. According to FDA’s OIG report, most of the clinical trials surrounding all subjects under FDA’s INDs took place outside the USA, and accordingly need translation services.
When bringing a new drug to market, translation is required along with being culturally adapted. Moreover, introducing a new drug includes a lot of stages that need translation such as clinical research, regulatory submissions, manufacturing, multicultural marketing, and also packaging.
The Translation Gate is a leading pharmaceutical translation service provider in the United States, the Middle East, Asia, and Africa.
Acting as primary support for Pharmaceutical companies and Clinical Research Organizations (CROs) by translating their critical documents. Delivering error-free documents which are accurately reviewed by certified Clinicians and doctors.
- Informed Consent Forms
- Brochures
- Case Reports
- Protocol Documents
- Packaging text
- Label Text
- Training Docs
- Synopses
- Scientific Articles
- Leaflets
- Clinical Trials
- Protocols of clinical trials
- Scientific Articles
- Suspected Unexpected Serious Adverse Reactions (SUSARs)
- Package Inserts and Labels
- Patient Recruitment Materials
- Patient-Reported Outcome Measures (PROMs)
- Toxicology Reports
- Regulatory Documents
- Pharmacological Studies
- QoL Scales
- Endpoint Adjudication Documents
- Master Batch Records
- Marketing Collateral
- Product Labels
- Study Protocols
- Patient Source Documents, Admission and Discharge
- Pharmaceutical Bulletins
- Documentation for Regulatory Agencies
- Clinical Study Reports
- Manuals for Research Laboratories
- Market Surveys
- Dossiers
- Development Safety Update Reports (DSURs)
- Datasheets
- Drug Registration Documentation
- Adverse Event Source Documents
- Case Report Forms (CRFs)
- Instructions for Use (IFUs)
- Patient Diaries
