Francesca Caselli

Francesca Caselli Email and Phone Number

Regulatory Affairs Specialist @ IBSA Italy
Milan, IT
Francesca Caselli's Location
Milan, Lombardy, Italy, Italy
Francesca Caselli's Contact Details

Francesca Caselli phone numbers

About Francesca Caselli

Francesca Caselli is a Regulatory Affairs Specialist at IBSA Italy. She possess expertise in farmacovigilanza, regulatory submissions, sop, ricerca clinica, regulatory affairs and 21 more skills. She is proficient in Francese, Tedesco and Inglese.

Francesca Caselli's Current Company Details
IBSA Italy

Ibsa Italy

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Regulatory Affairs Specialist
Milan, IT
Francesca Caselli Work Experience Details
  • Ibsa Italy
    Regulatory Affairs Specialist
    Ibsa Italy
    Milan, It
  • Ibsa Italy
    Regulatory Affairs Specialist
    Ibsa Italy Nov 2023 - Present
    Lodi, Lombardia, Italia
  • Farma 1000 Importazione E Distribuzione In Italia Di Prodotti Farmaceutici Per Uso Umano
    Regulatory Affairs And Quality Specialist
    Farma 1000 Importazione E Distribuzione In Italia Di Prodotti Farmaceutici Per Uso Umano Dec 2019 - Nov 2023
    Milano, Lombardia, Italia
  • Guna S.P.A.
    Regulatory Affairs Specialist And Pharmacovigilance Qppv
    Guna S.P.A. Jul 2015 - Dec 2019
    Milano, Italia
  • Guna S.P.A.
    Regulatory Affairs And Pharmacovigilance Specialist
    Guna S.P.A. Oct 2014 - Dec 2019
    Milano, Italia
  • Guna S.P.A.
    Regulatory Affairs Assistant
    Guna S.P.A. Jul 2014 - Sep 2014
    Milano, Italia
  • Laboratoires Boiron
    Regulatory Affairs And Pharmacovigilance Assistant
    Laboratoires Boiron Apr 2012 - Jun 2014
    Segrate Milano
    Archiving information about regulatory and pharmacovigilance records, tracking due dates of routine submissions and deadlines of the office activity.Preparing and submission of variation and deficiency letters for homeopathic and allopathic medicinal products.Labelling for homeopathics, food supplements, cosmetics.Review of scientific and technical information documents, advertising to the general public and institutional site.Homeopathic medicinal… Show more Archiving information about regulatory and pharmacovigilance records, tracking due dates of routine submissions and deadlines of the office activity.Preparing and submission of variation and deficiency letters for homeopathic and allopathic medicinal products.Labelling for homeopathics, food supplements, cosmetics.Review of scientific and technical information documents, advertising to the general public and institutional site.Homeopathic medicinal dossierPharmacovigilance: redaction of internal SOP, self managing pharmacovigilance reports ( ADR collection, data management, follow up...), review of PSUR made by pharmacovigilance head office, preparing and giving presentation to large audience for pharmacovigilance personnel training. Show less
  • Laboratoires Boiron
    Regulatory Affairs Intern
    Laboratoires Boiron Oct 2011 - Apr 2012

Francesca Caselli Skills

Farmacovigilanza Regulatory Submissions Sop Ricerca Clinica Regulatory Affairs Industria Farmaceutica Pharmacovigilance Norme Di Buona Fabbricazione Fda Biotecnologia Strumenti Medicali Farmaceutica Microsoft Office Pharmaceutical Industry Ectd Farmacologia Microsoft Excel Vendite Farmaceutiche Regulatory Requirements Gestione Dei Dati Requisiti Regolamentari Homeopathy Gmp Ich Guidelines Food Supplements Medical Devices

Francesca Caselli Education Details

Frequently Asked Questions about Francesca Caselli

What company does Francesca Caselli work for?

Francesca Caselli works for Ibsa Italy

What is Francesca Caselli's role at the current company?

Francesca Caselli's current role is Regulatory Affairs Specialist.

What is Francesca Caselli's direct phone number?

Francesca Caselli's direct phone number is +3933935*****

What schools did Francesca Caselli attend?

Francesca Caselli attended Università Degli Studi Di Firenze.

What skills is Francesca Caselli known for?

Francesca Caselli has skills like Farmacovigilanza, Regulatory Submissions, Sop, Ricerca Clinica, Regulatory Affairs, Industria Farmaceutica, Pharmacovigilance, Norme Di Buona Fabbricazione, Fda, Biotecnologia, Strumenti Medicali, Farmaceutica.

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