Sally Anliker

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Sally Anliker is the director of regulatory affairs CMC at Eli Lilly and Company

Articles

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Quality by Design for Biotechnology Products—Part 3

Sally Anliker;Jennifer Mercer;Tim Schofield;Bruce Meiklejohn;Mark Schenerman;Samantha Sheridan;Taruna Arora;Stefanie Pluschkell;Meg Casais;Mark Rosolowsky;Joseph Mezzatesta;Paul Tsang;Jim Precup;Stuart Feldman;Lois Atkins;Bernerd McGarvey;Tony Lubiniecki;Paul Smock;Jutta Look;Anurag S. Rathore
January 1st 2010

Regulatory flexibility can make continuous improvement possible.

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Quality by Design for Biotechnology Products—Part 2

Sally Anliker;Jennifer Mercer;Tim Schofield;Bruce Meiklejohn;Mark Schenerman;Samantha Sheridan;Taruna Arora;Stefanie Pluschkell;Meg Casais;Mark Rosolowsky;Joseph Mezzatesta;Paul Tsang;Jim Precup;Stuart Feldman;Bernerd McGarvey;Tony Lubiniecki;Paul Smock;Jutta Look;Anurag S. Rathore
December 1st 2009

Second in a three-part series that discusses the complexities of QbD implementation in biotech development.

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Quality by Design for Biotechnology Products—Part 1

Sally Anliker;Jennifer Mercer;Tim Schofield;Bruce Meiklejohn;Mark Schenerman;Samantha Sheridan;Taruna Arora;Stefanie Pluschkell;Meg Casais;Mark Rosolowsky;Joseph Mezzatesta;Paul Tsang;Jim Precup;Stuart Feldman;Lois Atkins;Bernerd McGarvey;Tony Lubiniecki;Paul Smock;Jutta Look;Anurag S. Rathore
November 1st 2009

First in a three-part series that discusses the complexities of QbD implementation in biotech product development.

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