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
32%
Breakthrough designations
11%
Protecting the supply chain
37%
Expedited reviews of drug submissions
11%
More stakeholder involvement
11%
View Results
Jim Miller Outsourcing Outlook Jim Miller Health Systems Raise the Bar on Reimbursing New Drugs
Cynthia Challener, PhD Ingredients Insider Cynthia ChallenerThe Mainstreaming of Continuous Flow API Synthesis
Jill Wechsler Regulatory Watch Jill Wechsler Industry Seeks Clearer Standards for Track and Trace
Siegfried Schmitt Ask the Expert Siegfried SchmittData Integrity
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