by
Rebecca Stauffer, PDA | Nov 04, 2019
American Pharmaceutical Review
Aug. 27, 2019
“Product Temperature Monitoring and Control via Thermal Imaging during Continuous Freeze-Drying of Pharmaceutical Unit Doses”—Pieter-Jan Van Bockstal, Jos Corver and
Thomas De Beer
BioPharm International
Aug. 1, 2019
“Moving From Compliance to Quality”— Agnes Shanley
Cleanroom Technology
Sept. 6, 2019
“How to design a cleanroom monitoring system”—Hasim Solmaz
Healthcare Packaging
Oct. 4, 2019
“Particles in Parenterals: 2019 Update”—Dirk Rodgers
International Pharmaceutical Quality
Oct. 29, 2019
“USP Views Early Broad Stakeholder
Engagement as Essential in Developing
Performance-Based Standards for Biologics”—(includes summaries of talks from 2019 PDA/FDA Joint Regulatory Conference)
Maas & Peither GMP Publishing
July 23, 2019
“PDA Annual Meeting 2019 – Part 1”—Thomas Peither
Pink Sheet
Aug. 20, 2019
“Pfizer/Mylan: Pending Clash Of Quality
Systems Could Determine Fate Of New Firm”—Bowman Cox
Sept. 20, 2019
“FDA: Key FY 2019 Warning Letter Trend Is
Inadequate Testing For API Impurities”—Joanne Eglovitch
Oct. 8, 2019
“Manufacturing Quality United States
Some Pointers From The US FDA On How To
Conduct Better Out-Of-Spec Investigations”—Joanne Eglovitch