For additional details see: Ī Wright Path’s experienced team will execute and navigate the FDA and global regulatory requirements and submissions so you can launch your product into the marketplace confidently.Īgilis Consulting Group is your trusted human factors partner for the global medical market. Our medical and pharmaceutical translators and interpreters provide confidential translations of multilingual documents for regulatory submissions to the FDA and other regulatory agencies worldwide translations of Clinical Trial Protocol (CTP), clinical trial data and summaries Summaries of product characteristics (SPCs) Instructions for Use (IFU) medical records physician reports manuals for medical devices articles for medical journals life sciences patents, and other documents. provides multilingual medical, pharmaceutical, legal document translation and interpreting services from and into Simplified Chinese, Korean, French, German, Traditional Chinese, Italian, Japanese, Korean, Brazilian Portuguese, Spanish, European Portuguese, Hebrew, Arabic, Norwegian, Turkish, Greek, Swedish, Dutch, Finnish, English, and other foreign languages.
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