Developments in life sciences and the medical field are racing forward at an exponential pace. As research in the field grows increasingly technical and multi-disciplinary, organizations are finding it difficult to have all the information and potential collaborators they require close at hand.
With the penetration of new markets, the added challenge of growing regulatory compliance and communication of complex product information in dozens of languages is becoming an important factor.
Coupled with the stringent requirements demanded by life science and medical companies, these imperatives are threatening to limit the expansion of such strategic industries.
Find out how Verztec can assist leading life science and medical organizations with a unique combination of linguistic excellence, technical expertise, quality management systems and project coordination practices.
Verztec’s capabilities extend to the various types of source documents:
- Medical and clinical software applications
- User Interfaces for medical devices
- Patient Information Sheet
- Patents
- Clinical trials
- MSDS (Material Safety Data Sheets)
- Scientific tenders
- Medical reports and literature
- Marketing Communications
- Websites, Extranet and Intranet sites
- User Guides and Manuals
- Medical Record Forms
- Standard Operating Procedures
- Contracts and Agreements
- Medical Trial Transcription
- Interpretation
- Ethics, Compliance and Regulatory Documentation
- Medical research reports and clinical trial protocols
- Patient information papers
- Psychology papers
- Medical prescriptions and diagnoses
- User guides for medical staff and patients
- Instruction manuals, brochures and software for usage of medical equipment
- Clinical, toxicological, pharmacological and biological documents
- Medical questionnaires and medical terminology glossaries