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The author reviews the draft guidance on process validation, its QbD applications, and its potential impact on sterile manufacturing operations. Individuals working in pharmaceutical sterile ...

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 ...

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 ...

Lee, MA, March 28, 2023 (GLOBE NEWSWIRE) -- Berkshire Sterile Manufacturing (BSM), a fill finish CDMO located in Lee, MA, recently completed their first GMP fill using their new low loss fill process.

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 ...

Interested in a career with an excellent job growth forecast that also provides the reward that you are helping your fellow ...

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 ...

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 ...

Lee, MA, May 18, 2023 (GLOBE NEWSWIRE) -- RNAimmune, a biotech company focused on developing groundbreaking mRNA therapies, recently received FDA approval to begin Phase 1 clinical studies for an ...