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Adeodata can perform Assessment on your systems in compliance with the relevant regulations, such as:

  • GxP, ICH, FDA 21CFR Part 11, EU Annex 11
  • GAMP, PIC/S (record and electronical signatures management)
  • MHRA, FDA, WHO, PIC/S, EMA Q&A (Data Integrity)


The assessment procedure is structured in three steps and consists in defining:

  • the current situation (AS IS)
  • the desired future situation (TO BE)
  • the potential corrective actions (TO DO)
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