Sigridur Harpa Hafsteinsdottir

Regulatory Affairs Manager at ProductLife Group

Sigridur Harpa Hafsteinsdottir is a Regulatory Affairs Manager at ProductLife Group since April 2018. Prior to this, Sigridur Harpa worked as a Regulatory Affairs Specialist CMC at Teva/Actavis Generics from August 2013 to March 2018. Sigridur also has experience as a Researcher at the Icelandic Heart Association from August 2006 to September 2013. Sigridur Harpa holds a Master of Science in Human Biology from the University of Copenhagen and a Bachelor of Science in Molecular Biology from Háskóli Íslands.

Location

Reykjavík, Iceland

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ProductLife Group

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ProductLife Group’s SOS approach helps clients navigate through the outsourcing journey by streamlining business processes and aligning them with information management models. The approach extends to the management and governance of data through a regulatory information management approach that cuts across functions such as chemistry,manufacturing, and control; regulatory; and safety—to align information that has been created by different people at different times and for different objectives.


Headquarters

Courbevoie, France

Employees

501-1,000

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