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Simple solutions for complex projects
We have been working closely alongside public and private organisations in the life-sciences sector for thirty years, and we are well aware of the sensitive nature of this field.
We have built up experience and acquired the necessary linguistic know-how and terminological resources to provide high-precision medical and pharmaceutical translation services.
Having Intrawelt® as your partner means placing your trust in skilled professionals who are aware of the sector requirements and who are able to guide you towards optimal solutions.
The methodological rigor and increased confidentiality required for pharmaceutical translation are ensured by TÜV Italia certified process controls.
Certified translation
Compliance certificates
Sworn translations
Legalisation
Apostille
Consular certifications
Chamber of Commerce certifications
Medicine and Life science
Scientific articles
Clinical studies
Abstracts
Manuals and usage instructions
Treatment records
Medical/Legal reports
Medical test results and analysis
Scientific university theses
Patents
Training and instruction materials
Patient documentation
Medical and scientific websites
Reports
Safety data sheets
Technical/scientific documentation
Pharma
Package leaflets
Summary of Product Information documents
Labelling
Bilingual FIT forms
Standard Operating Procedures (SOP)
Quality manuals
Regulatory and quality assurance documents
Ministerial authorisations and manufacturing authorisations
Pharmacovigilance documents
Master Batch Records (MBR)
Marketing materials
Registration dossiers and Common Technical Documents (CTD)
Production reports, deviation reports, Working Instructions (WI)
Analysis and process validation documents
Product monographs and technical files
Stability studies and risk analyses
Packaging materials documentation
Registration certificates, MA renewals, OTC certificates, Pharmaceutical product certificates
Documentation for centralised EMA products
Inspection reports and Medicines Agency communications
Scientific research
Clinical protocols
Information sheets
Informed consent declarations
Patient cards
Study documents
Patient questionnaires
Clinical studies
Privacy and data processing policies
Procedures and contracts with clinical institutions
Agreements with CROs