Scientific programme · profiles under review

The speakers

Portrait of Dott. Massimo Scaccabarozzi

Chair of Unindustria’s Pharmaceutical and Biomedical Section and Past President of Farmindustria

Dott. Massimo Scaccabarozzi

A Pharmacy graduate of the University of Milan, he served for over 20 years as President and Chief Executive Officer of Janssen Italia (Johnson & Johnson) before taking on the role of Director of ON RADAR, the think tank of Fondazione Menarini. Chair of Unindustria Lazio’s Pharmaceutical and Biomedical Section, he was President of Farmindustria from 2011 to 2022 and is a member of its Executive Board. Among his various appointments, he also served as President of Fondazione Roma Expo 2030.

  • Keynote lecture
Portrait of Pier Luigi Agazzi

Active member of AFI and GAMP Italia · CEO of Adeodata

Pier Luigi Agazzi

An Electronic Engineering graduate of Politecnico di Milano, he holds a master’s degree from MIP and pursued further studies in expert systems at MIT in Boston. He has worked in process control systems engineering since 1985, focusing on pharmaceutical compliance at STERIL from 1992. Since joining Adeodata in 2000, he has specialised in the validation of computerised systems for production, laboratories and business management. He conducts audits, Data Integrity assessments and training.

  • Computerised System Validation
  • Data Integrity
Portrait of Antonio Altobelli

Lecturer at Baxter Academy · CEO of ABC Consulting

Antonio Altobelli

A consultant and designer specialising in cytotoxic drug compounding units (UFA), with over 35 years of experience in the pharmaceutical sector and more than 50 UFA facilities designed. A lecturer and author of technical and scientific publications, he is recognised as one of Italy’s leading experts in integrating facility design, automation, robotics and GMP requirements for sterile compounding laboratories. He is the author of the white paper Robotica e allestimenti antiblastici in UFA.

  • UFA
  • Robotics
  • GMP Annex 1
Portrait of Diego Bompadre

Sales Director · QSGroup

Diego Bompadre

A manager and contamination control specialist with over twenty years of experience in the pharmaceutical sector. Sales and EMS Director at Rigel Life Sciences, he is a recognised expert in the design of continuous monitoring systems and the application of GMP Annex 1 requirements. An active member of ASCCA, PDA and ISPE, he has authored studies on air quality and teaches training courses on sterility assurance in laboratories.

  • Contamination control
  • Continuous monitoring
  • FMS
  • Sterility assurance
Portrait of Mirko Gabriele

CEO of Infinite Vision · PDA Past President

Mirko Gabriele

A professional and researcher specialising in pharmaceuticals and biotechnology, with a strong scientific background (PhD) focused on innovation and development. Experienced in managing complex projects and applying regulatory requirements, he combines theoretical knowledge with practical expertise to optimise industrial processes and quality systems. He is recognised for his ability to integrate advanced technological solutions into sterile and controlled environments.

  • Artificial intelligence
  • Quality
  • GMP processes
  • Innovation
Portrait of Cristina Da Valle

GMP specialist at Adeodata

Cristina Da Valle

A professional with over twenty years of experience in the pharmaceutical sector, with expertise in microbiology, sterility assurance and GMP quality systems. She has worked in multinational environments, focusing on microbiology laboratories, sterile drug manufacturing and regulatory compliance. She now supports Life Science companies in applying GMP, with a particular focus on Contamination Control Strategy, Annex 1 and microbiological risk management.

  • Sterility assurance
  • Microbiology
  • CCS
  • GMP Annex 1
Portrait of Irene Mella

GMP specialist at Adeodata

Irene Mella

A Biomedical Engineer with experience in the pharmaceutical, biotech and chemical sectors, Irene Mella specialises in the qualification, validation and GxP compliance of facilities, equipment and computerised systems. She has contributed to Computer System Validation, Equipment Qualification and Cleaning Validation projects, supporting Life Science companies in applying regulatory requirements. She combines engineering and regulatory expertise with a pragmatic approach to compliance and digitalisation.

  • Validation
  • Equipment Qualification
  • CSV
  • GxP

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