Translation Services
Translation services play a crucial role in clinical trials, regulatory processes, and business development, particularly in global scenarios and when dealing with non-English-speaking populations and regulatory bodies.
Accurate and consistent translations of study-related materials are crucial in clinical trials and regulatory processes to ensure participant understanding, compliance with regulatory requirements, and successful study outcomes. Take advantage of Credevo to seek professional and specialized translation services.
Type Of Translation Services
| Translation Services for Clinical Trials |
| Translation services play a critical role in clinical trials by enabling effective communication between researchers, sponsors, and participants from diverse linguistic and cultural backgrounds. |
| Translation Services for Regulatory Affairs |
| Accurate translations of regulatory documents, such as marketing authorization applications, labeling, & safety reports, are necessary for the successful submission and approval of new products. |
| Translation Services For Marketing, Promotional & Business Development |
| Accurate and culturally appropriate translations of business proposals, contracts, and presentations can help build trust, establish credibility, and expand business opportunities globally. |
Need support for translation services?
Credevo offers a comprehensive range of pharmaceutical translation services to meet all your linguistic needs, from clinical trial documents and regulatory filings to marketing and business development materials.
Global Pharmaceutical Translation Service
We understand that each region has unique linguistic and cultural nuances. Therefore we offer specialized translation services for different regions, including Europe, North America, Latin America, Asia-Pac, and the Middle East.
Our translation team of expert linguists and subject matter experts ensure that translations are not only accurate but also culturally appropriate for the target audience.
The Type of Documentation We Support In Translation
- Adverse Event Source Documents
- Case Report Forms (CRFs)
- Data Sheets
- Development Safety Update Reports (DSURs)
- Dossiers
- Drug Registration Documentation
- Endpoint Adjudication Documents
- Informed Consent Forms
- Insert Leaflets
- Instructions for Use (IFUs)
- Marketing Collateral
- Master Batch Records
- Package Inserts and Labels
- Patient Diaries
- Patient Recruitment Materials
- Patient Reported Outcome Measures (PROMs)
- Patient Source Documents, Admission, and Discharge, Labs
- Pharmacological Studies
- Product Labels
- QoL Scales
- Regulatory Documents
- Scientific Papers
- Study Protocols
- Suspected Unexpected Serious Adverse Reactions (SUSARs)
- Toxicology Reports
- Adverse Event Source Documents
- Data Sheets
- Development Safety Update Reports (DSURs)
- DossiersDrug Registration Documentation
- Endpoint Adjudication Documents
- Insert Leaflets
- Instructions for Use (IFUs)Marketing Collateral
- Master Batch RecordsPackage Inserts and Labels
- Patient DiariesPatient Recruitment Materials
- Patient Reported Outcome Measures (PROMs)
- Patient Source Documents, Admission, and Discharge, Labs
- Pharmacological Studies
- Product Labels
- QoL Scales
- Regulatory Documents
- Scientific Papers
- Study Protocols
- Suspected Unexpected Serious Adverse Reactions (SUSARs)
- Product labeling and package inserts
- Scientific articles and publications
- Marketing and advertising materials, including brochures, flyers, and promotional emails
- Training manuals and presentations for sales representatives and medical professionals
- Market research reports and surveys
- Website content, including product information and online marketing materials
- Medical conference presentations and abstracts
- And many more.
Connect with us to explore our services
Mail your queries to inquiry@credevo.com or contact us in other ways.