Clinical Research translation for Global Healthcare
Quality That
Resonates Globally
Adapting to Your Research Needs
Every clinical trial is unique, and so are its translation needs. We offer translation solutions that adapt to the specific requirements of your research, whether it’s the scale, complexity, or linguistic challenges involved.
Supporting Research through Innovation
Adaptive clinical trials require adjustments based on emerging data. We provide translation services that are responsive and efficient, enabling quick updates to trial documents as the research evolves.
Translations Aligned with Global Data Regulations
Data privacy is a critical concern in clinical research, especially in cross-border trials. We ensure that all translations align with international data privacy regulations like GDPR, safeguarding participant information and maintaining compliance.
Specialized Terminology
Rare disease research often involves highly specialized terminology. Our expert translators have the knowledge and experience to handle these complex terms, ensuring that research findings are accurately communicated to all stakeholders.
Consistent Training Across Borders
Global clinical trials require consistent training for all team members, regardless of location. We translate training materials, ensuring that all researchers, clinicians, and support staff understand the protocols and procedures, fostering a cohesive approach.
Translations That Keep Participants Engaged
Participant retention is vital for the success of clinical trials. Our translations help maintain clear and ongoing communication with participants, ensuring they feel informed and engaged throughout the trial, reducing dropout rates.
Our Proven
Translation Process
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Types of Clinical Research
Documents We Translate
- General Consent Forms
- Pediatric Consent Forms
- Assent Forms for Minors
- HIPAA Authorization Forms
- Phase I-IV Protocols
- Adaptive Trial Protocols
- Protocol Amendments
- Investigator’s Brochures
- Quality of Life Questionnaires
- Symptom Diaries
- Patient Satisfaction Surveys
- Adherence Logs
- New Drug Applications (NDA)
- Investigational New Drug Applications (IND)
- Clinical Trial Applications (CTA)
- Marketing Authorization Applications (MAA)
- Adverse Event Reports
- Risk Management Plans
- Periodic Safety Update Reports (PSUR)
- Pharmacovigilance System Master Files (PSMF)
- Study Protocols
- Ethical Review Board Applications
- Investigator Declarations
- Patient Information Sheets
Helping Your
Research Go Global
100+ Languages, Affordable Prices
Start Your Clinical Research
Translation Journey
AI-Complemented Human Translation
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