About ToxHub

Carla Landolfi (ERT)

Founder – Chief Executive Officer Toxicology Risk Assessor

• Over 25 years of experience in toxicology, including 8 years managing the Toxicology Group in the pharmaceutical industry. 

• Expertise in developing safety programs for pharmaceuticals, cosmetics, food supplements, medical devices, biocides, and other consumer products. 

• In-depth knowledge of regulatory guidelines (ICH, EMA, FDA, GLP, ISO) and contributor to peer-reviewed journals as an author and invited speaker at international conferences. 

• Professor in university master’s programs and Founding Editor of Archives of Clinical Toxicology. 

Maria Labianca  

Regulatory toxicologist​ Medical Device and Consumer Products Specialist​  Certificated Cosmetic Safety Assessor

(SICC)​

• Experience in toxicology and production field gained in the pharmaceutical industry. ​

• Qualification of Cosmetic Safety Assessor issued by SICC (Italian Society of Chemistry and Cosmetic Sciences).

• Expert in Medical Device safety assessment.​

Chiara Gazerro  ​

Regulatory toxicologist​, Chemical Risk Assessment Specialist – Pharma&Chemical Business Units

• Master of science MSc in chemistry and pharmaceutical technology from university of Trieste; graduating with an experimental thesis in in vitro toxicology.
• Qualified pharmacist.
• Specialized in Chemical Risk Assessment and Management (SSVGRC) at Sapienza University of Rome.
• Qualification as RSPP Modules A, B and C, pursuant to Italian Legislative Decree 81/2008.
• Expert in human and environmental risk assessment for pharmaceutical products, impurities, and chemicals.
• Computational Toxicology

Giorgina Mangano (EuCP)

Senior Scientific Consultant
Biologist and Pharmacologist

• Over 30 years of experience in pharmacology, including 9 years managing the in vitro Preclinical Development team in the pharmaceutical industry. 

• Expertise in drug discovery and preclinical development for CNS, inflammation/pain, anti-infectives, and other therapeutic areas, as well as cosmetics, food supplements, and medical devices. 

• Strong knowledge of regulatory guidelines (ICH, EMA, FDA, GLP, ISO) and extensive experience with systemic and topical formulations. 

• Published author of peer-reviewed papers, co-inventor on international patents, and certified European Pharmacologist (EuCP) since 2003. 

Eleonora Pace  ​

Regulatory Toxicologist – Medical Devices Business Unit

• Master of science MSc in chemistry and pharmaceutical technology from university of Rome La Sapienza; graduating with a thesis in molecular oncology;
• Research assistant a University of Copenhagen at Physiological pharmaceutics group, focusing on developing an oral delivery formulation for a BCS4 drug.
• Qualified pharmacist.
• Continuing education by attending a 2nd level Master dreee at Università Cattolica del Sacro Cuore in Rome. Title: Preclinical and Clinical Drug Development: Technical-Scientific, Regulatory, and Ethical Aspects.
• Expert in Medical Device safety assessment.​