This letter / 01
Raghav Chandra
Indian generics companies often present USFDA remediation spending as a one-off that investors can add back. That presentation teaches boards to under-fund the laboratory that decides whether a plant may sell at all.
Every few months an Indian generics company announces that a USFDA inspection has gone badly. The quarterly results that follow have a familiar shape. Consultants' fees, retesting, additional staff and write-offs of batches on hold are grouped together and presented as remediation costs. Analysts add them back. Management speaks of a temporary disruption. A year or two later, if the site clears, the costs vanish from the commentary as though they had been weather.
