Drug Master File (DMF) Registration in China
Video Overview:
GRP has successfully registered over 50 DMFs in China and is your trusted partner in China to help you from guiding with the NMP process for DMF registration, be your legal business representative in China and ensure successful registration of DMF in time.
With our office in Shanghai and global team of regulatory experts, we can support with technical documentation, NMPA consultation and regional operational support in submitting the dossier to NMPA as well as responding to all the queries to NMPA on your behalf.
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More Resources:
Drug Master File (DMF) in China
https://globalregulatorypartners.com/case_studies/dmf-registration-in-china-for-a-leading-us-based-api-manufacturer/
https://globalregulatorypartners.com/countries/asia/china-national-national-medical-products-administration-nmpa/