Pharmaceutical Technology, October 2012 Issue (PDF)
Integration of Less-Formal Risk Assessment Tools into Change Control
Technical Forum: Disposable Chromatography
Uniformity of Dosage Units Using Large Sample Sizes
Early Development GMPs for Small-Molecule Specifications: An Industry Perspective (Part V)
Quality by Design for Analytical Methods: Implications for Method Validation and Transfer
Advancing Protein Crystallization: Microgravity Effects and Predictive Models
Determining Potency of Preclinical Dose Formulations
Tools in Waiting: Time for Evolutionary Operation
Outsourcing Pharmaceutical Infrastructure Operations
Obtaining Stable Homogenous Mixtures with Micronized APIs