The new cleanroom at our global headquarters in Salt Lake City, Utah, was designed for today's rigorous contamination control expectations, driven by EU GMP Annex 1. Learn More
Cleaning validation requirements for reusable medical devices according to AAMI TIR30 did not distinguish between non-critical devices on the one hand and semi-critical or critical devices on the other. Additionally, many validation testing requirements were formulated using generalities rather than...
Cleaning validation requirements for reusable medical devices according to AAMI TIR30 did not distinguish between non-critical devices on the one hand and semi-critical or critical devices on the other. Only general recommendations were formulated, which resulted in one validation approach...
Ensuring that reusable medical devices can be properly cleaned, disinfected, and/or sterilized is imperative to ensure patient safety and to minimize healthcare-acquired infections, corrective actions, and recalls. Regulatory agencies and healthcare facilities are increasingly concerned about the spread of diseases,...
SALT LAKE CITY, UT – January 31, 2014 – Nelson Laboratories (www.nelsonlabs.com) will conduct two classes for medical device manufacturers at the 2014 MD&M West Conference Feb. 12 beginning at 10:00 a.m. in room #208AB covering the most up-to-date information...
SALT LAKE CITY – Jan. 31, 2014 – Nelson Laboratories (www.nelsonlabs.com) will conduct two classes for medical device manufacturers at the 2014 MD&M West Conference Feb. 12 beginning at 10:00 a.m. in room #208AB covering the most up-to-date information on...
