Overview documents of drug registration

Drug R&D and Registration Data cover research project initiation reports for new drugs, research review, drug clinical trial protocol, investigator’s brochure, standard operating procedures, case report, clinical study report and drug registration data review (pre-clinical, clinical and pharmacological section);

Drug Safety Reports cover serious adverse events (SAE) reports, periodic safety reports (PSUR) and translation, sorting and writing of safety information on foreign medicines.

Registration documents of medical devices

Medical device operating manual, user’s guide and safety report.

Polishing and translation for SCI medical papers

Provide accurate amendments for expression and translation of papers in accordance with the requirements of target academic journals submitted by the clients for the language expression of the paper to ensure that the English language expression of the papers is professional and authentic and meets the requirements of language level of overseas publications.

Keynote speech draft

Apply professional knowledge and experience to write and revise in accordance with standard forms of professional presentation, and produce them in the form of the presentation required by the client.