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Rachel Turow

Rachel Turow is a highly accomplished professional with a diverse educational background and extensive experience in regulatory law and policy.

She holds a Doctor of Jurisprudence in Law from the University of Michigan Law School, a Master of Public Health in Public Health from the University of Michigan, and a Bachelor of Arts in Biology from Stanford University.

Currently, Rachel serves as the Associate General Counsel for Regulatory Law and Policy at Teva Pharmaceuticals, where she also heads U.S Regulatory Policy.

Prior to her current role, she held the position of Executive Counsel - Regulatory Law at Teva Pharmaceuticals.

Rachel has also acted as a Council Member at Glg (Gerson Lehrman Group) and served as the Director of Regulatory Policy at Novo Nordisk.

Her previous experience includes roles such as Regulatory Counsel and Special Assistant at the FDA, Associate Counsel and Director of Legal Affairs at United Therapeutics, and Summer Associate positions at Weil, Gotshal & Manges Llp, Jones Day, and United Therapeutics.

With her strong educational foundation and comprehensive legal and regulatory expertise, Rachel Turow is a valuable asset within the pharmaceutical and healthcare industries.

She is known for her strategic approach to regulatory challenges and her contributions to shaping regulatory policies.

Rachel's commitment to public health, combined with her legal acumen, makes her a respected figure in the field.

Rachel Turow
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Location

Washington, District Of Columbia