Sterile product manufacturing and related testing have evolved significantly during the last 30 years. From requirements for acceptance criteria for media-fill tests, to developing validated ...
Microorganism lethality requirements for process validation must always be balanced with the need to protect product integrity and patient safety. Submitted: Feb. 9, 2015. Accepted: May 29, 2015.
The update to EU GMP Annex 1 offers market opportunities in aseptic operations, focusing on compliance with new standards. Key areas include contamination control, cleanroom design, and advanced ...
1. In a story on respect for sterile processing: Operating room teams should treat sterile processing staff with respect to achieve optimal patient safety and employee satisfaction outcomes, according ...
PORT WASHINGTON, N.Y., March 30, 2011 - Pall Corporation (NYSE: PLL) is launching an innovative solution for convenient and secure sterile separation of flexible tubing assemblies. The single-use Pall ...
Central sterile processing is essential for a safe and efficient operating room. Mistakes in sterilization can cause delays in surgery and patient infections, among other issues. Alecia Cooper, RN, BS ...
Why is aseptic processing important in pharmaceutical manufacturing? The manufacturing of both sterile drugs and biological products can be achieved through terminal sterilization or aseptic ...
Interested in a career with an excellent job growth forecast that also provides the reward that you are helping your fellow ...
The following content is sponsored by Surgical Directions. Most hospitals in recent years have focused needed attention on preventing surgical site infections. Properly timed antibiotics, skin ...
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