The Safe Finishing of your Sterile Product

Drug Master File (DMF)

A DMF type III has been registered at the FDA since 2009. It contains the relevant information regarding the seal design, manufacturing and processing.

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

DMF Letter of acces request

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

1. Applicant information

This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.