Labiana's range of outsourcing services permit our clients to carry out quick and efficient registration processes of pharmaceutical products for Europe and the main worldwide markets.
We prepare reports that includes all the documentation and trials as required by current legislation.
Preparing technical product files for pharmaceutical specialities
Creating technical files including documentation and clinical trials according to the current regulations.
Monitoring necessary clinical trials for the corresponding phases within the registration file (wether researching new products or Galenic Developments, developing manufacturing methods of producing pilot batches and process validations).
All of these dossiers are complying with the EU regulatory requirements.
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