Sidley Welcomes Former FDA Combination Products Subject Matter Expert Jay Jariwala

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WASHINGTON, D.C.—Sidley is pleased to welcome Jay Jariwala, Senior Director, Regulatory Compliance, to the firm’s Food, Drug, and Medical Device Compliance and Enforcement practice. He joins the firm’s Washington, D.C. office from the U.S. Food and Drug Administration (FDA), where he served most recently as Team Leader/Combination Products subject matter expert in the agency’s Center for Drug Evaluation and Research, Office of Compliance, Office of Manufacturing Quality (CDER/OMQ).

Jay will rely upon his more than 13 years of agency experience to help the firm’s life sciences clients—including drug, biologics, and medical device manufacturers—prepare for regulatory inspections, address regulatory inspection observations, assist in developing and executing remediation plans, respond to FDA compliance and enforcement actions, and provide guidance on interactions with the FDA.

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