Sinopep has sufficient experience in filing and submitting documents to authorities both home and abroad. The Chemical, Manufacturing and Control (CMC) documents provided by Sinopep, such as DMF (drug master file),enable the competent authorities (e.g. FDA, EMA) to review the information of API, in order to evaluate issuing Marketing Authorization to drug applicants. In addition to submitting registration documents in the United States and Europe, Sinopep also has rich experience in registration declaration in China.