Doc On Call? Cosmetic Manufacturers May Need M.D. On Retainer Under MoCRA

Cosmetic manufacturers’ recordkeeping and reporting responsibilities under the Modernization of Cosmetic Regulations Act that kick in at year’s end may require hiring a medical professional to delineate serious from minor adverse events, says attorney David Abramowitz.

A partner in Locke Lord, LLP’s Chicago office, Abramowitz discussed the 29 December 2023 deadline by which each cosmetic product manufacturer’s responsible person must keep records of all adverse events and report to the US Food and Drug