In accordance with the current pharmaceutical regulation, a finished dosage form has to be released by a laboratory in European territory, prior to its placing on the market at any country of the Union.
What is needed for these studies?
For this activity, the authorization as import laboratory, the GMP certification and the authorization as pharmaceutical distributor are needed.
What Netpharmalab offers to you…
At Netpharmalab, we have the authorizations and certification needed as well as more than 2,000 sqm of warehouse for the import of finished product from the manufacturer country.
We offer an integral service so that we take care of the storage, sampling, analysis, release and distribution of the batches ensuring the GMP and GDP compliance.