GxP Cleaning Standards: What Facilities Need to Know
While all industries are regulated to some extent, few are as regulated as those of biotechnology, medical device manufacturing, and pharmaceuticals. These regulations leave very little, if any, room for error. A single microscopic particle or mistake in sanitation...
Contamination Control 101 Best Practices for ISO 7 & ISO 8 Cleanrooms
When dealing with research and manufacturing in an ISO 7 and ISO 8 cleanroom environment, there’s often a very fine line between success and costly failure. Often, the causes of these failures can’t even be seen by the human eye. That’s because even very small...
Audit‑Ready Facilities Preparing for FDA & ISO Cleanroom Inspections
Hearing the word “audit” is enough to send many professionals into a state of panic. That said, audits are not only necessary, but they are also vital to facilities that utilize cleanrooms. While facility managers may find audits stressful, this test of their...
Why ISO 9001:2015 Certification Matters for Biotech Facility Cleaning
When it comes to biotechnology and biotech research, one small unaccounted-for variable or error can have a serious impact on a project. Whether you’re developing a new life-saving medication or researching the human genome, the environment your team is working in...