Raw materials and finished products must be analysed according to a set of specifications that have to be fulfilled to be considered suitable for their use in the manufacture of drug products (in the case of raw materials) or to be placed in the market (in the case of the finished products).


What is needed for these studies?

The GMP certification and to have que equipment qualified and the systems validated are needed to carry out the release analysis.

What Netpharmalab offers to you…

At Netpharmalab, we carry out the release analysis with the highest quality standards.

We have equipment for the physicochemical and microbiological release of every pharmaceutical dosage form: solids, semisolids, liquids, sterile products, etc.

We prepare the certificates of analysis and the certificates of conformance and we are able to import, release and distribute drug products for their commercialization in the European market.