What kind of missions?
Coordination and external monitoring of
pharmaceutical development activities for new dosage
forms, range extensions, update of existing
submissions: project assessment, analytical
sub-contracting, review of development results, etc…
Preparation and writing of modules 3.2.S
and 3.2.P of Common Technical Documents (CTDs) and
corresponding Quality Overall Summaries (QOS)
Search for partnerships (acquisition,
subcontracting, licensing)
Development of raw materials: synthesis
intermediates, quality review and preparation of
monographs for pharmaceutical compounds (excipients
and drug substances), substances for cosmetic use
Literature survey and preparation of
summarized documentation regarding
chemical/pharmaceutical development
Sourcing of raw materials
Attendance to professional exhibitions
and scientific congresses (scientific support, market
intelligence)