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When a downstream pharmaceutical manufacturer submits an application for pharmaceutical registration, it may submit an application for formulator exemption, which requires the signature of the holder of the original drug registration certificate before it can be used.
Manufacturers that have obtained drug registration can submit a notice to EPA of changing the supplier of the original drug, along with the relevant application form, and do not need approval to change. It is worth noting that the method of use of the original drug registration needs to be consistent with the product of the preparation, while not chang
The source of the original drug used in the United States preparation registration certificate is confidential information, so the information cannot be obtained through public means.
There is no difference between the registration number of the United States subpacking registration Certificate and the registration number of ordinary registration.