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Audits Manufacturing Sites and Warehouses

The compliance with the current regulations is an essential aspect to obtain authorisations and to market products. Periodical evaluations of the compliance and business status is the first step to contain future issues and reduce regulatory costs and time.

Di Renzo Regulatory Affairs has a special unit including qualified experts fully committed to auditing and inspecting activities in all the sectors reported below.

Auditing activities are carried out based on the applicable regulations, including Good Manufacturing Practice (GMP), Good Pharmacovigilance Practice (GVP), Good Distribution Practice (GDP), Farmindustria Guidelines on Scientific Information, UNI CEI EN ISO 13485, UNI EN ISO 9001, UNI EN ISO 22716, HACCP etc.


  • ISO 9001 audits

Medicinal Products

  • GMP audits to finished product and active pharmaceutical ingredients (APIs) manufacturing sites, in Italy and in EU and extra-EU countries
  • Audits to MA holders, concessionaires, warehouses, wholesalers of medicinal products
  • Audits to MA holders for the Farmaindustria certification on the scientific information guidelines
  • GVP audits in pharmacovigilance to MA holders and concessionaires

Medical Devices

  • UNI CEI EN ISO 13485 audits
  • Audits to manufacturers, warehouses, distributors, wholesalers


  • UNI CEI EN ISO 22716 audits
  • Audits to companies and suppliers of cosmetics or ingredients
  • Audits to warehouses, distributors, wholesalers


  • Audits to companies and suppliers of PMCs and/or biocides
  • Audits to warehouses, distributors, wholesalers

Food Supplements

  • HACCP audits
  • Audits to companies and suppliers of food supplements and food for special medical purposes
  • Audits to warehouses, distributors, wholesalers

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