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Pharmaceutical Sciences, Manufacturing & Marketplace Report April 10, 2013


  From Cynthia Challener, PhD, Editor, Pharmaceutical Sciences, Manufacturing & Marketplace Report
Welcome to the fourth edition of the Pharmaceutical Sciences, Manufacturing & Marketplace Report, a new biweekly newsletter of Pharmaceutical Technology and BioPharm International, and an exclusive feature of the new Pharmaceutical Technology/BioPharm International Marketplace, an online community focused on products and services for drug development and manufacturing, which will launch in April 2013. The Pharmaceutical Sciences, Manufacturing & Marketplace Report provides insight in five main communities: solid dosage, semisolid, and specialty dosage forms; parenterals; chemical API manufacturing; biologic API manufacturing; and pharmaceutical analysis.

In this issue, given that the Parenteral Drug Association is having its annual meeting this month, our feature story focuses on parenterals, and specifically recent advances in freeze-drying. Several leading cell culture media manufacturers discuss how they are improving the quality of their products and learning more about the impact that media has on protein expression and therapeutic cell production. You can also find out about the latest advances in particle analysis and the chemistry behind taste masking in solid dosage forms.
 
 

       
       
Parenterals
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Maria Toutoudaki/Getty Images
Lyophilization Technology: Slow Progress but Hopeful Outlook

As an important method for improving the stability of parenterals, lyophilization is fairly well understood, but can still benefit from several advancements in the technology. Click Here to Read More

Join our Parenterals Linked-In Community
 
Biological API Manufacturing
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Maciej Frolow/Getty Images

Media Makers Focus on Quality

With high productivity achieved, makers of cell-culture media are working to optimize product quality through better understanding and control of raw materials and production processes.Click Here to Read More

Join our Biological API Manufacturing Linked-In Community
 
Pharmaceutical Analysis
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Adam Gault/Getty Images

Particle Characterization is Critical for Drug Performance

Iterative and multiple incremental advances in particle-characterization technology are making a difference in pharmaceutical analysis applications. Click Here to Read More

Join our Pharmaceutical Analysis Linked-In Community
 
Chemical API Manufacturing
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Alfred Pasieka/Getty Images

Navigating the Global Manufacturing Supply Chain

As the strategic value of emerging markets increase, pharmaceutical companies increase their R&D and manufacturing investments. Click Here to Read More

Join our Chemical API Manufacturing Linked-In Community
 
Solid, Semisolid, and Specialty Dosage Forms
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Ion-Bogdan Dumitrescu/Getty Images

Ignorance is Bliss in Solid Dosage Taste-Masking

The trick to taste-masking in solid dosage forms is to never let the taste buds have a chance. Click Here to Read More

Join our Solid, Semisolid, and Specialty Dosage Forms Linked-In Community

Highlights from Pharmaceutical Technology and BioPharm International
Recent articles from Pharmaceutical Technology and BioPharm International

Solid Dosage, Semisolid, and Specialty Dosage Forms

Solving Tableting and Tooling Problems (Pharmaceutical Technology)

Adopting a seven-step process to maintenance and storage improves tableting quality. Click Here to Read More



Chemical API Manufacturing

The Weaknesses and Strengths of the Global API Market  (Pharmaceutical Technology’s Sourcing and Management)

Supply-demand fundamentals show strong growth for generic APIs as gains in innovator APIs lag. Click Here to Read More



Parenterals

Seeking Cold-Chain Efficiency (Pharmaceutical Technology)

Medication safety and efficacy depend on maintaining products at the proper temperature. Click Here to Read More



Biological API Manufacturing

Therapeutic Antibodies in Review (BioPharm International)

Innovative products and a range of indications drive the therapeutic antibody market. Click Here to Read More



Pharmaceutical Analysis

Determination of Surface Visible Residue Limits on Pharmaceutical Plant Equipment (Pharmaceutical Technology)

The minimum amount of residue that can be visually detected is demonstrated for a small number of active pharmaceutical ingredients (APIs) on a range of different surface materials.Click Here to Read More



 
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Perspectives from Cynthia Challener, PhD, editor of the Pharmaceutical Sciences, Manufacturing & Marketplace Report and industry members

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