Annex 1

What’s One SOP or Protocol You Wish Every Cleanroom Leader Would Rethink

Too many cleanroom teams still assume that more disinfectant is the answer, but Annex 1 makes it clear that residues left behind can quietly undermine even the most aggressive cleaning regimes. Without a deliberate residue breakdown step—such as a validated rinse—bioburden can persist beneath the surface, driving CFU formation and downstream environmental monitoring failures….

Annex 1 Cleaning

Annex 1 didn’t merely refine regulatory language—it fundamentally reshaped expectations around how cleanrooms are cleaned, emphasizing contamination control strategies, residue-free performance, and repeatable processes that work right the first time. As manufacturers adjust, tools and materials like advanced ultrafiber technologies are becoming essential because they support consistent first-pass cleaning without shedding or compromising sterility….

Innovation and Excellence in Life Sciences: Benchmark Products’ Year in Review

A pharmaceutical manufacturer's advanced cleanroom operations and FDA-compliant bioprocessing solutions set new industry standards for durability and chemical r

One Year of The Exceeding Your Benchmark Podcast

A year of industry conversations reveals the critical manufacturing challenges reshaping life science and pharma operations