Manufacturing, Aseptic Processing

Feb 08, 2017
By BioPharm International Editors
Modular Automated Sampling Technology (MAST) allows direct aseptic transfer of bioreactor samples to analytical devices, providing rapid and reliable data in bioprocessing.
Feb 01, 2017
BioPharm International
Susan Schniepp, distinguished fellow at Regulatory Compliance Associates,  discusses how to ensure sterility when manufacturing small-scale parenteral batches.
Jan 09, 2017
By BioPharm International Editors
The company was cited by FDA for violations of sterile processing GMPs.
Jan 01, 2017
BioPharm International
Excipient selection strongly influences lyophilization performance for biologic drugs.
Dec 01, 2016
BioPharm International
John Ward, vice-president of Engineering at Patheon, discusses the potential for cross contamination in the manufacture of biopharmaceuticals.
Oct 02, 2016
BioPharm International
Susan Schniepp, distinguished fellow at Regulatory Compliance Associates, discusses the assessment of risk in the processing of intravenous injectable drugs.
Oct 01, 2016
BioPharm International
Laser-induced fluorescence, a rapid microbiology method for real-time airborne particle and microbial monitoring, enhances sterility assurance in pharmaceutical manufacturing.
Sep 23, 2016
By BioPharm International Editors
Wells Pharmacy Network is voluntarily recalling all of its products due to sterility concerns.
Sep 14, 2016
By BioPharm International Editors
FDA sent a warning letter to an Illinois compounding pharmacy for violations of the Federal Food, Drug, and Cosmetic Act.
Sep 01, 2016
BioPharm International
Improvements to aseptic manufacturing procedures are long overdue. But how feasible is it for manufacturers to modernize fill lines of legacy products?
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