Lisa’s experience covers the product lifecycle, from early development to post marketing support. Working with drug development companies she has provided clinical regulatory support which has involved IMPD and IB authoring as well as preparing and submitting CTAs. Lisa recently headed up a Value Engineering and Complexity Reduction project, co-ordinating a multinational’s in-house and external teams, developing and executing global variation strategies, project timelines and implementation plans. Lisa’s experience covers the product lifecycle, from early development to post marketing support. Working with drug development companies she has provided clinical regulatory support which has involved IMPD and IB authoring as well as preparing and submitting CTAs. Lisa recently headed up a Value Engineering and Complexity Reduction project, co-ordinating a multinational’s in-house and external teams, developing and executing global variation strategies, project timelines and implementation plans.
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