Pharmaceutical Effluent Testing
(40 CFR 439)

We have the ability, experience, and certifications to meet all your Pharmaceutical Manufacturing Industry (PMI) analytical needs.

Since the final EPA ruling 1998, we’ve provided the Pharmaceutical industry with professional project management, coordination of sampling supplies, and the highest level of data quality available to meet the 40 CFR 439 requirements.

We’re NELAP accredited (# E87661) and New Jersey ELAP approved and can provide a full range of analytical services including:

- EPA 1666A Volatiles by Isotope Dilution GC/MS
- EPA 1671A Volatiles by GC/FID
- EPA 524.2 Volatiles by GC/MS
Helpful Links
EPA: Federal Register: Pharmaceutical Manufacturing Category Effluent Limitations Guidelines, Pretreatment Standards, and New Source Performance Standards; Final Rule
http://www.epa.gov/EPA-WATER/1998/September/Day-21/w21027.htm
Wastewater Monitoring for the Pharmaceutical Manufacturing Industry fact sheet