A Risk-Based Approach to Stainless Steel Equipment Maintenance
Pumping Fluids in Biopharmaceutical Processing
Moving Forward with Adaptive Licensing
Collaboration Key to Meeting Excipient GMP Requirements
Regulatory Reform Is Not That Simple
Mass Spec Sheds New Light on Biologics Drug Development
Evaluating E&L Studies for Single-Use Systems
Characterization of Small-Molecule Drug Substances in Type II DMFs Supporting ANDAs
Ensuring Sterility in Small-Scale Production
Viewpoint: Challenges and Opportunities for CDMOs
User Fees Needed to Help FDA Manage its Full Plate
Cold Chain: Zeroing In on the Last Mile
Last-mile temperature control
Advancements in Extrusion-Spheronization
Establishing Blend Uniformity Acceptance Criteria for Oral Solid-Dosage Forms