Regulatory compliance is the key to acquiring product licenses and the cornerstone to access new markets. The regulatory translation is the translation of documentation on the approval and compliance of medical devices, pharmaceuticals and in vitro diagnostics products. From chemical to manufacturing, medical device to clinical research, healthcare to pharmaceutical, MedTrans offers high-quality regulatory translation services to meet regulatory compliance worldwide. Our experience and expertise will help you ensure your medical documents are approval-ready and meet the local regulatory standards with all language requirements.