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Demonstrated expertise in chemistry, bioanalysis, immunoassay, chromatography and mass spectrometry.
Seven years of experience as a Scientist in Analytical Chemistry and a Scientific writer working for the pharmaceutical industry: professional translations and writing of Standard Operating Procedures, bioanalytical protocols and reports, Quality Audit reports, clinical protocols, toxicological study plans, scientific publications, extraction and synthesis procedures, instrument manuals, software validation documents.
Freelance translations of Material Safety Data Sheets according to REACH, GHS, CLP regulations, assay kit manuals, technical manuals, tourism advertisement, web-sites, video games.
Deep knowledge of the guidance and regulations which are followed in the pharmaceutical industry such as FDA guidance, GLP, ICH and GHS regulations.