Sterile products processing relates to how sterile drug products are manufactured using aseptic (or free from contamination) process methods where the drug substance, excipients, and vehicle (e.g., saline or water for injection) are combined and filled into a container (such as a syringe)
Guidance Documents
Manufacturing Operations (1)
Microbiological & Viral Contamination Control (1)
Community Discussions
Community Discussions
Feb 16, 2025
Workforce of the Future
Feb 15, 2025
Manufacturing Operations
Feb 13, 2025
Manufacturing Operations
Oral Solid Dosage
Feb 10, 2025
Sustainable Facilities, HVAC, & Controlled Environments
Feb 06, 2025
Feb 03, 2025
Jan 30, 2025
Webinars
iSpeak Blog Posts
Pharmaceutical Engineering® Magazine
Videos
Professional Development Training
Aseptic Processing & Annex 1 Training Course
This course will focus on aseptic processing and quality management around the most important pharmaceutical technology.
White Papers
July / August 2024
The explosive growth of advanced therapy medicinal products (ATMPs), particularly cellular…
May / June 2024
The commercialization of personalized medicine has ushered in demand for a new type of facility—…
March / April 2024
Navigating the Asia Pacific Pharmaceutical Landscape for Global Impact Cover: The Asia Pacific…
