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Features
Sharing Supply-Chain Security
A panel of industry and regulatory experts, including FDA, discuss efforts to secure the global pharmaceutical supply chain. This article contains bonus online-exclusive material.
Developing a modified Pulsincap system
Chronotherapeutic drug delivery systems (CRDDS) have been recognized as potentially beneficial to the chronotherapy (timeoptimized therapy) of widespread chronic diseases that display time-dependent symptoms.
Whatever Happened to Classical Chemistry?
A recent book reminds readers that small-molecule chemistry has enabled advances in biotechnology.
Trends in labelling
Following years of development, DataMatrix codes are now a viable labelling solution for pharma manufacturers.
Challenges and Strategies for Implementing Automated Visual Inspection for Biopharmaceuticals
The authors used a light-transmission-based static division system to detect particles of foreign contaminants in prefilled vials.
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2009 aaps showcase
USP and USAID Launch New Program to Improve Drug Quality
European Regulators Take Action to Improve Public Information Access
Repairing the Engine of Drug Innovation
Is Big Pharma Choosing Patients over Patents?
Moving Stem-Cell Therapy to the Clinic

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Industry Leaders: Q+A
Hans Engels of DSM Pharmaceuticals
Engels discusses the latest industry developments and trends.
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Events
November 8, 2009 - November 12, 2009
2009 AAPS Annual Meeting and Exposition
November 8, 2009 - November 11, 2009
2009 ISPE Annual Meeting
November 9, 2009 - November 10, 2009
FDA Inspections: What To Expect And How To Prepare
Regulatory Corner
Standards & Regulations
Insider Solutions: A New Direction for USP?
With a five-yar revision cycle around the corner, USP will hit or miss the collaboration mark.
Regulatory Update: The IPEC Novel Excipient Safety Evaluation Procedure
The authors, representing the International Pharmaceutical Excipients Council, propose a new evaluation procedure, including tiered toxicology testing for excipients.
Safety versus Speed in Drug Development
The heightened focus on risk raises concerns about delays in approving new drugs.
Regulatory Roundup: FDA Issues Guidance on In Vitro Diagnostic 2009 H1N1 Tests, More...
Also, FDA and WebMD increase collaboration and PPD is awarded contract to evaluate the agency's postmarket spontaneous-adverse-event surveillance system.
Jim MillerOutsourcing OutlookJim Miller Facing Reality
Patricia Van ArnumIngredients InsiderPatricia Van Arnum Advancing Chiral Chemistry in API Synthesis
Faiz kermaniSpotlightFaiz Kermani Demographic time bomb
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