2021-05-19 11:26 The prospect of overseas opportunities drives medical device firms to develop medical device products. It requires careful translation of all instructions and specifications to market your medical devices in a new country. The complicated process of ... дальше
2021-05-19 11:25 Scientific publishing continually evolves as discoveries, technical advances, vendors, and data become known. Translating academic content requires in-depth knowledge of the subject material plus fluency in the source and target languages. MedTrans u ... дальше
2021-05-19 11:25 Informed Consent Forms (ICFs), setting out information about a clinical trial and its conduct, are essential in gaining the patient’s written consent to participate in the trial by signing the document. The guidelines used to create ICFs are based on ... дальше
2021-05-19 11:25 During the drug development and approval process, good clinical practice and regulatory compliance demand careful recording of clinical and non-clinical data in documents. Investigator's Brochure (IB) are complex documents that provide investigators ... дальше
2021-05-19 11:25 Translation services are becoming an indispensable component along with the increasing demand for conducting multi-country clinical trials. The clinical trial follows a carefully controlled protocol, a study plan that describes what will be done in t ... дальше
2021-05-19 11:25 Clinical Study Reports (CSRs) are critical means by which regulators can assess the outcome of clinical studies. Their format and content are defined in Guideline for Industry Structure and Content of Clinical Study Reports (ICH E3). A clinical study ... дальше
2021-05-19 11:24 A case report form (CRF, or case study report form) is a paper or electronic questionnaire specifically used in clinical trial research to facilitate data analysis and test hypotheses. The case report form is the tool used by the sponsor of the clini ... дальше
2021-05-19 11:24 Product Information (PI) is an intrinsic part of the application for marketing authorization of a new drug or medicine. In the European Union, it includes the Summary of Product Characteristics (SmPC) and the Package Leaflet (PL); it names the author ... дальше
2021-04-22 19:49 Translation services are becoming an indispensable component along with the increasing demand for conducting multi-country clinical trials. The clinical trial follows a carefully controlled protocol, a study plan that describes what will be done in t ... дальше
2021-04-22 19:49 Clinical Study Reports (CSRs) are critical means by which regulators can assess the outcome of clinical studies. Their format and content are defined in Guideline for Industry Structure and Content of Clinical Study Reports (ICH E3). A clinical study ... дальше