PTSM: Pharmaceutical Technology Sourcing and Management, Nov 10, 2009 - Pharmaceutical Technology

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PTSM: Pharmaceutical Technology Sourcing and Management, Nov 10, 2009
Biotech
Manufacturing and Regulatory Considerations in Biosimilars
By Patricia Van Arnum
Leading experts from an upcoming conference on biosimilars by the Drug, Chemical, and Associated Technologies Association share their insights on the manufacturing and regulatory considerations for biosimilars.
Global Feature
CPhI Exhibitors Announce Expansions
By Patricia Van Arnum
Exhibitors announce capacity expansions, service enhancements, and new products at CPhI Worldwide in Madrid.
Outsourcing
Sizing Up the CDMO Market
By Jim Miller
A new analysis highlights growth drivers and challenges for clinical supply-chain services.
Pharma Partner Focus
Vetter Expands Clinical-and Commercial-Scale Operations
By Patricia Van Arnum
Vetter moves ahead with a new development facility in the US and expanded capabilities in Germany.

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Survey
FDASIA was signed into law two years ago. Where has the most progress been made in implementation?
Reducing drug shortages
Breakthrough designations
Protecting the supply chain
Expedited reviews of drug submissions
More stakeholder involvement
Reducing drug shortages
70%
Breakthrough designations
4%
Protecting the supply chain
17%
Expedited reviews of drug submissions
2%
More stakeholder involvement
7%
View Results
Eric Langerr Outsourcing Outlook Eric LangerTargeting Different Off-Shore Destinations
Cynthia Challener, PhD Ingredients Insider Cynthia ChallenerAsymmetric Synthesis Continues to Advance
Jill Wechsler Regulatory Watch Jill Wechsler Data Integrity Key to GMP Compliance
Sean Milmo European Regulatory WatchSean MilmoExtending the Scope of Pharmacovigilance Comes at a Price
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