Illinois Administrative Code
Title 35 - ENVIRONMENTAL PROTECTION
Part 218 - ORGANIC MATERIAL EMISSION STANDARDS AND LIMITATIONS FOR THE CHICAGO AREA
Subpart T - PHARMACEUTICAL MANUFACTURING
Section 218.489 - Recordkeeping for Air Pollution Control Equipment
Current through Register Vol. 48, No. 38, September 20, 2024
a) The owner or operator of a pharmaceutical manufacturing source shall maintain the following records:
b) For any leak subject to Section 218.485 of this Part which cannot be readily repaired within one hour after detection, the following records shall be kept:
c) The following records shall be kept for emission units subject to Section 218.484 of this Part which contain VOL:
d) For each emission unit used in the manufacture of pharmaceuticals for which the owner or operator of a pharmaceutical manufacturing source claims emission standards are not applicable, because the emissions are below the applicability cutoffs in Section 218.480(a) or 218.480(b) of this Part, the owner or operator shall:
e) Records required under subsection (a) of this Section shall be maintained by the owner or operator for a minimum of two years after the date on which they are made.
f) Copies of the records shall be made available to the Agency or the USEPA upon verbal or written request.