Del Corno & associati takes care of the whole drug approval process, including:

• CTA applications for every clinical trial phase (phase I- IV) in Italy .

• Time and cost planning for regulatory activities: regulatory support to the most convenient regulatory approach.

• Regulatory support to developing companies.

• Redaction of EU CTD dossiers, including preparation of NeeS and eCTD dossiers.

• Lifecycle management of medicinal products: updates, variations and renewals.

• National and European registration and maintanance procedures (MRP and Centralized).

• Due diligences activities: licensing support.

• Pharmacovigilance.

• Regulatory/Pharmacovigilance Training.

• Readability Testing (User testing).

• Medical devices/Cosmetics support.



Common technical document
Marketing Authorisation
Lifecycle management
Readability testing/user testing
Regulatory support
Regulatory consultancy medicinal products

Del Corno & Associati S.r.l.

Milano, Via Padre Reginaldo Giuliani 10/A
  • Phone No.: +39.02.9285.3502
  • Fax: +
  • Mobile: +39.335.68.98.224


Services to the pharmaceutical industry, aimed at obtaining the appropriate authorizations in Italy and Europe.

Del Corno & associati is a regulatory consultancy providing services to the pharmaceutical industry, aimed at developing and obtaining the appropriate authorizations to market medical products, medical devices and food supplements.