Please find below contact details
and contact us today! Our consultants are always ready to help you.

Please find below contact details
and contact us today! Our consultants are always ready to help you.
Regulatory Authorities usually ask applicants to submit all technical documentation translated to Spanish.
Whether you require a specialist translation or proofreading only, we can help. We guarantee that the translation is accurate, appealing, and coherent.
Certificate to Foreign Government (CFG), Free Sale Certificate, ISO 13485 Certificate, ISO 14971 Certificate, and EC Certificate.
IEC certificates, EMC test report, safety test report, biocompatibility test report, clinical evaluation report, sterilization validation report, stability validation report, and more.
Declaration of Conformity (DoC), Certificate of Analysis (CoA), Instructions for Use (IFU), QC inspection reports, Risk Management Plan, Risk Management File, STEDs, FMEA, and more.
Human translator with a background in the pharmaceutical industry.
Qualitative assessment by a second native-speaking translator.
Check and modify texts in terms of technical terminology.
Your documents will be ready on time for regulatory submissions.