MedBioteQ also works with regulatory documents related to both drugs and chemicals. We strictly adhere to the EMA dictionary, templates & rules in terms of translation and update.

The documents we deal with in this area are, for example:

Summary of product characteristics (SmPC), packaging texts, patient information leaflets (PILs), marketing authorizations, market introduction texts, regulatory approval dossiers, Material Safety Data Sheet (MSDS), and all documents directly or indirectly linked to chemicals and drugs.