The FDA Guidance for Industry, “Container Closure Systems for Packaging Human Drugs and Biologics,” addresses the review and evaluation of packaging requirements.
By

Frances L. Degraziof

Enzymatic Therapy has relied on compact vibratory screeners to optimize product quality and production while meeting growing demand.
By Del Williams

- Nasal Drug Delivery: Linger of Gamma Scintigraphy Fragrance Likely
Assessment of Nasal Drug Delivery in Humans Using Radionuclide Imaging Techniques
By Abeer M. Al-Ghananeem and Peter A. Crooks

- Management Processes: Environmental Quality Assurance Failure to Recognize the Importance of each Process Component and to Properly Design an Appropriate System is a Major Defect of many Analytical Measurement Programs
By Henry Nowicki and Barbara Sherman

APIs

- Dealing with Insoluble Compounds: Mechanical Treatment of APIs to Reduce Particle Size can Lead to Increased Dissolution Rates in Water
By Kevin M. Kane, Ph.D.

LAB ANALYSIS

- Reoviruses as Cancer Therapeutics: Oncolytic Viruses will Most Likely Enter Clinical Practice as Adjunctive Agents to Conventional Chemotherapy
By Matt Coffey

- Single-Use Setup A One-Time System Makes for a Clean and Efficient Bioprocess Environments
By John Boehm

- Quality Systems Automation Software Helps Sanofi-Aventis with Compliance, Productivity Goals Data “Helped Us to Quickly Identify and Fix the Problem”
By Bonnie Haferkamp

- Records Management: Implementing FEA Records Management With a Systematic and Well-Planned Approach, Agencies can Deploy a Single Repository that can Service Core Applications that Meets or Exceeds Federal Requirements
By Kathleen Kummer

- What Can RFID Do for Pharma? RFID (Radio Frequency Identification) has the Potential to be a Powerful Tool for the Pharmaceutical Industry as a Means to Face New Supply Chain Challenges
By Bill Arnold