Dr. Marco Polizzi

Responsible for batch release in conformity to the local and international rules, for management and planning of production cycles, for the drafting of the sop and technical documents, for the site master file follow up, for personnel training, for recall management, for business development, for the follow up of existing MA, for purchaser audits and self-inspections, for communication with local and internationals authorities.

Regulatory Affairs: manteinance and renewal of ma, management of the products lifecycle and pharmaceutical dossiers variations, PSUR submission, preparation of database for the department, archives management, public affairs and merketing inquiries, technical documents management, contacts with local and international authorities.

manteinance and renewal of ma, pharmaceutical dossiers variations, psur updating, preparation of database for the department, archives management, public affairs inquiries.

Advanced pharmaceuticals technologies, quality assurance, pharmacovigilance, GMP, GLP, regulatory subjects.

Bachelor of Pharmaceutical Chemistry and Technologies.