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 project management
 clinical monitoring
 safety -    pharmacovigilence
 data management
 market research
 medical writing
 medical/scientific    translations
 clinical quality assurance

Safety review of CRFs in house by qualified personnel
Full reporting of SAEs following each Sponsor’s safety reporting SOPs and
Timely follow-up of all SAEs in close collaboration with all related parties
Complete pharmacovigilence services through collaboration with external specialists