Who we are



  • Donato Bonifazi (Trial Manager): MEcon, Degree in Management; certified Project Manager; Extensive experience in European Project Management; Business Consulting and Trial Management. Member of the Paediatric Working Group of the EUCROF (European Clinical Research Organizations Federation) and President of the Italian Association of Clinical Research Organization (AICRO). He is Coordinator of the TEDDY – European Network of Excellence for Paediatric Clinical Research, an independent multidisciplinary and multinational research Network (category 1 network member of Enpr-EMA), composed by 50 partners from 20 EU and non-EU countries aimed at facilitating the performance of good quality paediatric studies and research.
  • Mariagrazia Felisi (PHARM Sole Director): Degree in Life Sciences, PhD in Clinical Pharmacology and Medical Therapy and Master Degree in Pharmacovigilance. Several years of experience in Clinical Research.
  • Luca Forlani (Information Technology): IT Engineer with strong expertise in data management. He is also specialized in websites development and communication strategies.
  • Cristina Manfredi (Regulatory Affairs and Pharmacovigilance): BSc (Hons) in European Business with Technology, MA in Marketing Communications, Master in Bioethics for Clinical Trials and Ethics Committees. Experience in regulatory affairs and pharmacovigilance.
  • Rosetta Padula (Monitorng Activities): Degree in chemistry. Several years of experience in Clinical Research and CRA since 2013 in Pediatrics and rare diseases trials, medical device and observational study.
  • Gabriele Morselli (Business Development): Degree in Pharmacy. Several years of experience in Clinical Research, Project Management and Business Development. Collaboration with Phamraceutical Companies, Scientific Societies, Hospitals, Ethic Committees, Italian Key Opinion Leaders.
  • Giulia Chiaruttini (Clinical Research): MPharm and PhD in Immunology. Experience in clinical research (antibody discovery for oncology).
  • Mariapaola Felisi (Administrative office and Quality Assurance RGQ (ISO)): Responsible for administration and trial documentation archiving.
  • Bonka Georgieva (Administrative Management): Master degree in ‘Cooperative Management’. Expert in Project management and financing.
  • Silvia Pulici (Quality Assurance ICH-GCP): Degree in Pharmaceutical Chemistry and Technology. Long-standing experience in clinical trial management and monitoring activities.
  • Simona Ravera (Data Management): Degree in Life Sciences and Master Degree in Pharmacoeconomics. Experience in Outcomes Research, Helth Related Quality of Life, Health Economics, data entry and management.
  • Bianca Tempesta (Drug Management): PhD in Pharmacology and Toxicology, Master Degree in Industrial and Enviromental Biotechnology. Experinece in drug management and technical operation activities of multinational studies within EU-funded projects.