toxhub-consulting

ABOUT US

ToxHub is a group specialized in ensuring the safety of your products and their regulatory compliance with an extensive and proven track record in Toxicological Risk Assessment.

We are a dynamic and proactive consultancy company, with a broad range of toxicological expertise in the pharmaceutical, chemical and health care area.

Founded by toxicologists, with 25-years of experience in the pharmaceutical industry, ToxHub seeks to build on the broad experience of its principle consultants to provide tailored and cost-effective solutions to its customers, to solve their toxicological issues, to meet their needs and help support their business.

Our experts provide solutions to complex development, toxicological and regulatory issues, through the combined expertise of scientific and regulatory specialists.

carla landolfi

Carla Landolfi (ERT)

Founder – Chief Executive Officer Toxicology Risk Assessor

  • More than 20 years of experience in toxicology field gained in the pharmaceutical industry, 8 of them as Manager to the Toxicology Group.
  • Solid knowledge in the development of safety programs for pharmaceuticals, cosmetics, food supplements, medical devices, biocides and other consumer products.
  • Broad know how of regulatory national and international guidelines and rules (ICH/EMA/FDA/GLP/ISO).
  • Main or co-author of several papers and posters, published in peer-reviewed journals
  • Invited speaker at International Conferences.
  • Professor at university masters.
  • Founding Editor of Archives of Clinical Toxicology

Alberto Campana

Senior Toxicology Consultant
Biologist and Toxicologist

  • More than 40 years of experience in toxicology field gained in the pharmaceutical industry, 10 of them as Responsible to the Toxicology Department.
  • Solid knowledge in the development of safety programs for pharmaceuticals, cosmetics, food supplements, medical devices, and other consumer products.
  • Broad know how of regulatory national and international guidelines and rules
    (ICH/EMA/FDA/GLP/ISO).
  • Main or co-author of several papers and posters, published in peer-reviewed journals, and patents.
  • Co-inventor in several international patents.

Giorgina Mangano (EuCP)

Senior Scientific Consultant
Biologist and Pharmacologist

  • More than 30 years of experience in Pharmacology field gained in the pharmaceutical industry, 9 of them as Manager to the in vitro Preclinical Development team.
  • Degree in Biological Sciences, since 2003 member of Italian Society of Pharmacology (SIF), certified European Pharmacologist (EuCP).
  • Solid knowledge in the development of drug discovery and preclinical development programs for pharmaceuticals (mainly in CNS, inflammation/pain and anti-infectives therapeutic areas, systemic and topical formulations), cosmetics, food supplements and medical devices.
  • Broad know how of regulatory national and international guidelines and rules
    (ICH/EMA/FDA/GLP/ISO).
  • Main or co-author of several papers and posters, published in peer-reviewed journals.
  • Co-inventor in several international patents.

Maria Labianca

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

  • She has a master of science degree in chemistry and pharmaceutical thecnology from university of Trieste; and graduated with a thesis in toxicology, focusing on testing graphene derivates onto machropages.
  • She is also a qualified pharmacist.