• Brazil02:41
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  • Research
  • Clinical trials
  • Legal
  • Regulatory approval
  • Marketing/Sales
  • Training materials
Extensive knowledge in: New Drug Application (NDA) Files; Investigational New Drug (IND) Files; Reporting of Suspected Unexpected Serious Adverse Events (SUSARS); Incident Record Form (IRF); Medical History; Case report form (CRF); Scientific Articles; Regulatory guidance; GPM; SOP. In the last 3-4 years I’ve extensively worked with Clinical Trial Protocols, Patient questionnaires. Clinical study Reports, Ivestigator’s Brochure, New Drug Application (NDA) Files, IFUs, and Lab manuals.
Translated content of:
  • Abbott Laboratories
  • Advanced Chemical Industries
  • Alkaloid
  • Amgen
  • Astellas Pharma
  • AstraZeneca
  • Bausch & Lomb
  • Bayer Schering Pharma AG
  • Celgene
  • Covance
  • Daiichi Sankyo
  • F. Hoffmann–La Roche Ltd.
  • GlaxoSmithKline
  • Horizon Pharma
  • Janssen Pharmaceutica Products
  • Lundbeck
  • Merck & Co.
  • Mitsubishi Pharma
  • Novartis
  • Pfizer
  • Regeneron Pharmaceuticals
  • Sanofi
  • Sigma Pharmaceuticals
  • Takeda Pharmaceutical Co.
  • Teva Pharmaceuticals
Medical professional:
  • Physician's assistant

Credentials:

  • Università degli Studi di Milano:
  • Italian
  • Portuguese
  • Spanish
  • UNIMI:
  • Portuguese to Italian
  • English to Italian
  • English to Portuguese
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