Forced Degradation Studies for Biopharmaceuticals
Choosing Containment Strategies For Highly Potent APIs
Visions for the Future of Biopharma Manufacturing
Outsourcing of Biomanufacturing in 2016
Pharmaceutical Quality: Where Do We Need to Go from Here?
Reporting Quality Metrics to FDA
Significant Revisions and Updates to the European Pharmacopoeia
Upstream and Downstream Operations Can Impact Biologic API Uniformity
The Value of Saving Lives
Practical Approaches to Tech Transfer and Scale-up of Lyophilization Processes
A QbD Method Development Approach for a Generic pMDI
Waking up to Track-and-Trace Benefits
Tackling Moisture Challenges in Solid Dosage Manufacturing
Penetrometer for Quality Monitoring
Operator Stations Ensure Functionality