
Roberto La Forgia
Founder & CEO
Graduated with a degree in Chemistry and Pharmaceutical Technologies from University of Bari in 2001. Roberto has extensive international experience as Qualified Person, working with global, national and regional companies, healthcare and research institutions active in nuclear medicine. For the past 10 years, Roberto has been managing complex projects, focusing on regulatory issues and technical challenges of radiopharmaceutical production. Main field of interest is R&D of imaging and theranostic agents for cancer. Co-inventor of Italian PSMA Cold Kit technology for labeling with Ga-68 – Lu-177 – Ac-225.

Maria De Bari
Chief Operating Officer
Responsible for B2B technical services; coordinates the team in charge of validation, production and quality control of radiopharmaceuticals; manages the research and development activities of BFP research projects. As Quality Assurance Manager, Maria verifies and approves all technical documentation, both Production and Quality Control, ensures the high quality standards of the services provided.

Onofrio Porcelli
Administrative Manager
As Administrative Manager he deals with the reporting of project activities and the bureaucratic-administrative management for partnerships of which BFP is leader. As Project Manager he is responsible for coordinating the partners involved, to link operations and deliverables for all ongoing projects.

Giulio Pedone
Quality Control Manager
Responsible for Quality Control of radiopharmaceuticals. On the B2B side he plans and carries out analyzes on raw materials and finished products, in compliance with the highest quality standards of the radiopharmaceutical legislation. It is responsible for drawing up all technical documents relating to quality controls in both the chemical-physical and microbiological fields and for approving, by means of appropriate analyzes, the radiopharmaceuticals before their administration to patients.

Annamaria Camporeale
Quality Assurance Specialist
Supervisor of production processes and quality control, according to the GMP guidelines (EudraLex - Volume 4: Part I, “Basic Requirements for Medicinal Products”; Part III, “GMP related documents”), with particular attention to the Annex #1, Annex #13 and Annex #15.
Business management supervisor.
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