Illinois Administrative Code
Title 35 - ENVIRONMENTAL PROTECTION
Part 215 - ORGANIC MATERIAL EMISSION STANDARDS AND LIMITATIONS
Subpart T - PHARMACEUTICAL MANUFACTURING
Section 215.489 - Recordkeeping (Renumbered)
Current through Register Vol. 48, No. 38, September 20, 2024
a) The owner or operator of a pharmaceutical manufacturing plant shall maintain the following records:
b) For any leak subject to Section 215.485 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 sources subject to Section 215.484 which contain volatile organic liquid:
d) For each emission source used in manufacture of pharmaceuticals for which the owner or operator of a pharmaceutical manufacturing plant claims emission standards are not applicable because the emissions are below the applicability cutoff in Section 215.480(a) or (b), the owner or operator shall:
e) Records required under 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 upon verbal or written request.