Susan Bairnsfather entered the pharmaceutical industry
over 20 years ago with science degrees in pre-medicine
(human biology major and biochemistry major) and
computer science, and additionally postgraduate studies
in pharmacology. She worked for 7 years as a regulatory
associate, 10 years as a statistical programmer, and
2 years as a regulatory writer before establishing her own
company, EPharmaTech, in 2006. She now provides
consultant services as a regulatory writer, regulatory
publisher, and statistical programmer. Susan has wide
experience in writing the full range of preclinical and
clinical regulatory documents, including submissions for
the US, Canadian, and EU authorities. She is also
experienced in data analyses and in electronically
integrating documentation to the eCTD. She has been
active as a member, presenter, and work shop leader
for American Medical Writers Association (AMWA),
European Medical Writers Association (EMWA),
Drug Information Association (DIA), and the Pharma-
ceutical SAS Users Group (PSUG). She has additionally
participated in CDISC and in HL7 SPL initiatives..Designed by Susan Bairnsfather - maximized for Internet Explorer 8.0.
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