Professional data reporting team to provide pharmacy research materials to declare the one-stop service
■ Applicable to China declaration and global declaration
■ Provide separate IND CMC and NDA CMC data writing services
■ Provide registration regulatory advice, program design and technical guidance services to assist in site verification and regulatory audit
■ Use Fushi Pharmaceutical or third-party data to organize the filing materials
■ The file format is based on the CTD or CTA template
■ Traceability Version Control
■ English and Chinese translation services between the two languages