Drug Master File (DMF)

EMA ensures regulatory compliance for your product with our US FDA and NMPA China registered Type III DMF, containing all necessary product and manufacturing information.

Worldwide products certified

Drug Master Files (DMF) have been registered at the US-FDA and NMPA China, Chinese National Medical Products Administration authorities for EMA’s Push-Off product range.

Those files contain the relevant information regarding the seal design, manufacturing and processing.

For our customers who have to register their product at the relevant authorities, we provide the LOA (letter of access) to our DMF within 48 hours after reception of the duly completed request.


DMF Letter of access request

The fields with an asterisk are required to process your request.

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