Provide the preparation outline of application materials.
Sign a confidentiality agreement between both parties to protect the interests of the manufacturer.
Pre review the registration data, estimate the risk and put forward correction measures
Review, translation, improvement, preparation and submission of registration documents.
Follow up the whole process of registration, reply to questions raised by authority and submit supplementary documents

We support our domestic customers for searching the minority pharmaceutical excipients and we also could offer the customize service for the international customer of pharmaceutical intermediates.