Clinical research materials translation at Ciklopea is performed by professional linguists with the industry background and/or additional training in providing language services for a specific pharmaceutical or medical domain.
Our solutions are developed to deliver:
- Top quality
- Compliance with the target market regulatory standards
- Security and confidentiality
The quality of our translations is achieved through a highly developed translation process, designed to utilize the most of professional human knowledge and translation technologies and adherence to the industry quality standards.
All clinical research materials are translated by professional translators and editors who are familiar with therapeutic practices and procedures, EMA/FDA guidelines and/or the standards and preferred terminology of the target market regulatory agencies, as well as the and the appropriate version of ICD-10.
We at Ciklopea care take security and confidentiality of your materials seriously and execute our projects in accordance with the international information security standards such as ISO 27001:2013.
Ciklopea provides professional translation services of a wide range of CR materials including:
- Study protocols
- Communication with local regulators
- Informed consent forms (ICF)
- Patient reported outcomes (PRO)
- Case report forms (CRF)